chronic diseases. FL84, Inc. is a privately held early-stage company that is applying advanced biological and computational platforms to discover breakthroughs in detection of and intervention against the etiologies that drive progression from health to disease.
Our goal is to leverage our proprietary platforms to disrupt the current approach of treating chronic disease too late. We endeavor to provide true health care rather than sick care to individuals that are at risk of progressing to disease. Flagship Pioneering is a biotechnology company that invents and builds platform companies, each with the potential for multiple products that transform human health or sustainability. Since
its launch in 2000, Flagship has originated and fostered more than 100 scientific ventures, resulting in more than $90 billion in aggregate value. Many of the companies Flagship has founded have addressed humanity's most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.
Flagship has been recognized twice on FORTUNE's " Change the World" list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies, and has
been twice named to Fast Company's annual list of the World's Most Innovative Companies.
Learn more about Flagship at . Position Summary: We are seeking a Sr. Scientist of Computational Biology/Bioinformatics who is enthusiastic about developing, learning and applying computational skills to understand complex biological systems and their relationship to clinical state changes. The candidate will improve and apply FL84's methods to biological data, including single-cell/nuclei RNAseq, proteomics, spatial transcriptomics and clinical data. The role will focus on two main areas: (1) application of machine learning to uncover disease mechanisms and identify novel therapeutic targets; and (2) exploration and processing of large, multimodal datasets to develop pipelines for preemptive clinical discovery.
An ideal candidate will pride themselves on their ability to craft scientifically logical and creative stories out of complex data and convert them into executable experiments. The position will provide a unique opportunity to play a foundational role in the development of FL84's preclinical platform and treat diseases before they become a burden to the patient or the healthcare system. Key Responsibilities: Develop and apply bioinformatics, computational biology, and machine learning tools to generate insights and hypotheses from high-dimensional molecular datasets Work with FL84's biology team to interpret the output of computational tools in the context of specific disease areas Identify and incorporate internal and external datasets to address questions critical to FL84's core objectives and generate testable hypotheses Ideate on how to align time-series biological data with clinically relevant inflection points identified in electronic health records, clinical trials, or other sources Establish pipelines to process large-scale molecular datasets and prioritize targets for biological validation Develop clear, intuitive visualizations and communicate analysis results via presentations to a multi-disciplinary audience Cultivate a data-centric company philosophy by helping to maintain best practices for software development, data management, and infrastructure Monitor and evaluate new and emerging technologies and models and identify opportunities for collaboration within Flagship Pioneering companies, academia, and third parties Basic Requirements: Ph D in computational biology, bioinformatics, or related field with 5+ years of experience in Biotech/Pharma space Extensive Python programming experience, including performance tuning, debugging, and familiarity with standard scientific packages for single-cell data analysis.
Deep understanding of biology and ability to formulate and test relevant hypotheses from large-scale molecular datasets Proficiency with git, Docker and AWS Ability to independently lead and run research projects, while maintaining close communication with team members Excellent communication and presentation skills. Must be able to speak and ideate with multi-disciplinary team including biologists.
Must be able to think independently, work collaboratively and contribute to an active intellectual environment Preferred Requirements : Experience with time series analysis, causal inference, domain adaptation, transfer learning, multi-modal deep learning, and geometric deep learning (learning on graphs and/or manifolds) Familiarity with R/Bioconductor and Nextflow Experience working with reference biological databases and datasets (e. g. TCGA, UK Biobank) is a strong plus Experience with CMAP, LINCS or other perturbagen (e. g. small molecule, CRISPR, etc. ) induced transcriptomic databases At Flagship, we recognize there is no perfect candidate.
If you have some of the experience listed above but not all, please apply anyway. Experience comes in many forms, skills are transferable, and passion goes a long way. We are dedicated to building diverse and inclusive teams and look forward to learning more about your unique background. Recruitment & Staffing Agencies: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, " FSP" ) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering's internal Talent Acquisition team.
Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.
transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers. /working-with-us. At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science. In
oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change.
We bring a human touch to every treatment we pioneer. Join us and make a difference. Position Summary The Principal Scientist, CV Pharmacology will the lead pharmacology initiatives supporting our pipeline in Cardiovascular Drug Discovery. The position requires subject matter expertise in heart disease and the ability to work independently and collaboratively in a team-driven environment. The role involves people management and potential hands-on work in the laboratory,
as needed. The ability to provide input on the in vivo strategy of CV programs is vital to this role.
This position is based in Brisbane, CA. Key Responsibilities Supervise talented scientist staff with expertise in CV pharmacology, predominantly focused on cardiac in vivo physiology. Laboratory leadership via hands-on experimentation and troubleshooting; expert in cardiac mechanics using invasive hemodynamics and echocardiography; experience handling animals for disease heart research. Ensure smooth interactions and appropriate support levels to facilitate drug discovery progression within the working groups. Ensure appropriate interface with translational research and early development teams to ensure pre-clinical pharmacological testing supports molecule progression into the clinic.
Establish and implement a strategy to identify and validate new pharmacological models. Be a contributor to the overall drug discovery strategy development within CV Drug Discovery; past drug target leadership is a plus. Support compliance with institutional animal care and use policies. Day to day responsibilities include team management in the laboratory, data and protocol reviews, presentations to working groups and upper management, training staff in sophisticated CV experimental methods as needed, hands-on laboratory experimentation.
Manage the career progression of CV Pharmacology team, as needed. Write pharmacology reports and regulatory documents to support FDA filings. Contribute to the leadership of the CV Drug Discovery team; policy matters, recruitment initiatives, succession planning, diversity. backss pharmacological suitability of potential business development opportunities, as needed. Basic Qualifications Bachelor's Degree 8+ years of academic and / or industry experience Or Master's Degree 6+ years of academic and / or industry experience Or Ph.
D. or equivalent advanced degree in the Life Sciences 4+ years of academic and / or industry experience Preferred Qualifications & Experience Ph. D. or equivalent advanced degree in the Life Sciences Ph D; 4+ years of academic and / or industry experience. Hands-on role as needed; expertise in cardiac mechanics (hemodynamics and imaging modalities) Expertise in the field of CV Pharmacology with a strong focus on heart failure; understanding of sarcomere biology, physiology and related drug targets is a plus. Prior drug discovery expertise within an industrial setting is highly desirable.
Strong core belief in the care of animals; understanding of animal welfare ethics and policy. Understanding of KO and transgenic model creation. Demonstrated success in interfacing with development teams and team leaders. Demonstrated success in line-managing teams of scientists via direct reporting or dotted line management. Excellent verbal and written communication skills. Commitment to developing one's own leadership skills via participation in scientific management training. The starting compensation for this job is a range from $121,000 - $152,000 plus incentive cash and stock opportunities (based on eligibility).
The starting pay takes into account characteristics of the job, such as required skills and where the job is performed. Final, individual compensation is decided based on demonstrated experience. For more on benefits, please visit our BMS Careers site. Eligibility for specific benefits listed in our careers site may vary based on the job and location. Why You Should Apply Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as " Transforming patients' lives through science™ " every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to xyz X@.
Visit careers. /eeo-accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
of my knowledge. Job Description At Takeda, we strive to create an exceptional people experience for patients, communities, partners, and employees. As a patient-focused, values-based, R&D-driven global biomedical company, we know our decisions and actions affect people's lives.
We look to our values of Takeda-ism, which incorporates Integrity, Fairness, Honesty and Perseverance, and Patient-Trust-Reputation-Business as a guide in our decision-making process to ensure we do what's right - for our patients, our people and society. Are you ready to embark on a transformative journey with Takeda? Our paid 10-12-week summer internship program is designed to immerse you in a dynamic learning
environment, featuring a blend of developmental and social activities. As a Takeda intern, you'll have the opportunity to contribute to impactful projects that play a crucial role in shaping both our business and the well-being of patients.
This experience will not only allow you to apply your technical and business knowledge but also empower you to showcase your analytical strength and creative problem-solving skills. Seize this chance to gain hands-on experience, expand your skill set, and make a meaningful impact on the healthcare industry. We invite you to be a part of our innovative and collaborative team, where your contributions matter. For more information about Takeda, please
visit. Please note that Takeda does not provide intern housing or a housing stipend.
Project Outline: We are seeking a graduate student to join Takeda for an intern experience and become part of a multi-disciplinary drug discovery group with a mission to provide innovative therapies for GI diseases, including inflammatory bowel disease and chronic liver disorders. We are looking for a motivated candidate to analyze clinical and -omics data to support the understanding of IBD treatment response trajectories using machine learning, systems biology, and knowledge graph approaches. Key responsibilities: Perform clinical and multi-omics data integration/analysis, including single-cell and bulk transcriptomic data, to identify treatment response molecular predictors, and inform pathway/target mechanism of action.
Implement and validate interpretable AI/ML strategies to predict treatment response signatures. Implement graph-based analytical tools for multimodal data integration and modeling to explore complex biological relationships and networks. Mine and analyze prior-knowledge databases (e. g. biological pathways, networks), and biomedical literatures (utilizing NLP, LLM approaches) Provide written documentation for developed methods and workflows. Present scientific reports in internal meetings in all settings and with participants across all levels of the organization, as well as for external audiences.
How you will contribute: Exceptional interpersonal, verbal communication and writing skills. Deadline-driven with an elevated level of organizational and planning skills. Strong quantitative, analytical, problem solving and conceptual skills. Proven record of accomplishment of teamwork, adaptability, innovation, initiative, and integrity. Global mindset to grow in a diverse work environment. Requirements / Qualifications: Currently enrolled in a relevant graduate program in related scientific discipline (Computational biology, Computer science, Genomics, Biostatistics or Bioinformatics preferred) Strong analytical, and data interpretation and visualization skills Proficiency in programming languages commonly used in bioinformatics (e.
g. Python, R) Strong organizational and effective communication skills. Currently authorized to work in the US (United States) without sponsorship. Takeda does not provide sponsorship for internship positions. Available to work full-time (40 hours/week), within the core business hours of 8:00am - 5:00pm, for 10-12 weeks during the summer months.
Graduate, Ph D, MD student with completion of a minimum of one year of university studies Must be enrolled in school the semester following your internship with Takeda. Please note that Takeda does not provide intern housing or a housing stipend. The hourly pay rate range is $20.00 per hour - $46.00 per hour. The final pay rate offered for this internship may consider several factors including, but not limited to, location, skills, education, and experience. EEO Statement Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, interaction, interactionual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.
Locations Boston, MA Worker Type Employee Worker Sub-Type Paid Intern (Fixed Term) (Trainee) Time Type Full time
degrader compounds and drive drug discovery efforts for both platform and pipeline projects. You should be able to work independently while contributing to a team environment and manage several projects simultaneously. The successful candidate must stay current with applicable internal/external scientific literature and be able to analyze, document, and report data rigorously.
You should possess excellent communication skills and be proficient in presenting in front of groups. Join our team at Abbvie and contribute to ground-breaking research in the field of target protein degradation. Responsibilities: Independently conceive and execute rigorous scientific research to profile potency,
efficacy, and mechanism of action for degraders (including, but not limited to ternary complex formation and ubiquitination) utilizing plate-based biochemical/cellular assays and quantitative western blot Innovate by developing novel biochemical and cellular assays to support structure-activity relationship (SAR) studies for degraders Drive and contribute to pipeline projects in collaboration with Therapeutic Area and Platform biology leads.
Demonstrate a high level of initiative and proficiency in troubleshooting experiments and be an internal leader by example for high standards in data analysis and quality Maintain good written records of laboratory procedures and communicate research
findings in cross-functional project team meetings and publications.
Qualifications: Position will be filled at level commensurate with extent of education, experience, and accomplishments Scientist II: BS in Biochemistry, Biophysics, Molecular Biology, Cell Biology, or related field of Biological Sciences with typically 7+ years of experience or MS and typically 5+ years of experience Sr Scientist I: BS Biochemistry, Biophysics, Molecular Biology, Cell Biology, or related field of Biological Sciences with typically 10+ years of experience, MS and typically 8+ years of experience, or Ph D and typically 0+ years of experience Demonstrated track record of scientific achievement (publication/presentation record) Proven ability to develop, analyze, and interpret assays for interrogation of biological questions Proficiency in standard biochemical and/or cellular/molecular techniques such as TR-FRET, Alpha LISA, Western Blots, ELISA, and Nano BRET Expertise/background in ubiquitin proteasome system biology or targeted protein degradation preferred, but not required Experience in small molecule drug discovery in academia or industry preferred, but not required Excellent problem-solving and multi-tasking skills in a fast-paced environment Must be a team-player with strong oral and written communication skills Abb Vie is committed to operating with integrity, driving innovation, transforming lives, serving our community, and embracing diversity and inclusion.
It is Abb Vie's policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, interaction (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, interactionual orientation, marital status, status as a protected veteran, or any other legally protected group status.
while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic experts. As the world leader in serving science,
our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations! Discover Impactful Work: Possesses a thorough understanding of laboratory procedures and can reliably conduct complex analysis with increased independence.
Performs a variety of complex sample preparation and analysis procedures to quantitatively measure medical and biomedical compounds in a variety of formulations and/or biological matrices. Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications.
Enters data into databases and reports. Performs self-review for own data prior to QC submission.
A day in the Life: Performs a variety of complex sample preparation and analysis procedures to quantitatively measure medical and biomedical compounds in a variety of formulations and /or biological matrices for stability and analytical testing. Works with multiple functional groups to meet business needs. Plans and organizes work with periodic supervision. Sets up and maintains analytical instrumentation. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory procedures and guidelines. Ensures QA findings are addressed appropriately.
Aids and training to other team members. Problem solving, either independently or with assistance pertaining to extraction and/or instrumentation problems. Communicates project status to project leader. Performs work assignments accurately, and in a timely and safe manner. Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP). Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers.
Qualifications - External Keys to Success: Education Bachelor's degree or equivalent and relevant formal academic / vocational qualification Experience Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years). In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills, Abilities Preferred experience: HPLC and/or CGE experience, GMP documentation.
Demonstrated knowledge of multiple applicable techniques such as: HPLC, CGE, ELISA, PCR, and compendia testing. Biomedical Testing, Karl Fischer, UV-Vis, FT-IR, TOC Preferred experience: HPLC/UPLC and CGE Proficient in Microsoft Excel and Word Proven track record to interpret data by performing trend analysis Proven track record in technical writing skills Ability to independently optimize analytical methods Proven problem solving and troubleshooting abilities Good written and oral communication skills Time management and project management skills Ability to work in a collaborative work environment with a team Work Environment Thermo Fisher Scientific values the health and wellbeing of our employees.
We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role: Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner. Able to work upright and stationary and/or standing for typical working hours. Able to lift and move objects up to 25 pounds. Able to work in non-traditional work environments.
Able to use and learn standard office equipment and technology with proficiency. May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments. Able to perform successfully under pressure while prioritizing and handling multiple projects or activities. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need.
#Start Your Story with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
of my knowledge. Job Description About the role: At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on three therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide.
Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Scientist II, Quantitative Systems Pharmacology Modeler, Neuroscience in our Cambridge, Massachusetts or Fujisawa, Kanagawa office. As a Quantitative Systems Pharmacology Modeler in Neuroscience
Therapeutic Area - Scientist II working in the DMPK & Modeling team, you will be empowered to interface between drug discovery units, translational medicine, drug metabolism and pharmacokinetics, nonclinical drug safety, medical sciences, clinical pharmacology, clinical sciences, and pharmacovigilance to influence drug discovery and development.
How you will contribute: POSITION OBJECTIVES: Support global drug discovery and development by building systems models for novel therapeutic agents, including small molecules, oligonucleotides, biologics, to treat various neurological diseases including neurodegeneration and neuromuscular diseases. Collaborate with preclinical research and drug
discovery, translational medicine, drug metabolism and pharmacokinetics, nonclinical drug safety, medical sciences, clinical pharmacology, clinical sciences, and pharmacovigilance to develop mathematical models to understand the targeted biological pathways and exposure-response/safety relationship of novel therapeutic agents.
Formulate and implement team-engaged right modeling & simulation strategy to assist drug discovery and development, through establishing PK/PD relationships and create mechanistic systems pharmacology/toxicology models to support project needs in forward and reverse translational manners. In-depth understanding of pharmacokinetics, pharmacology, biochemistry, immunology, numerical methods, as well as hands-on experience with modeling software, and ability to clearly present modeling and simulation findings.
POSITION ACCOUNTABILITIES: Design and build translational PK/PD/efficacy and mechanistic and/or systems models to assist with drug candidate selection, translational human pharmacologically active/efficacious dose prediction, safety margin selection, study design optimization and biomarker selection. Minimum Requirements/Qualifications: Ph. D/Pharm. D/M. D with training in chemical or biomedical engineering, medical sciences, mathematics, statistics, or equivalent area with at least 2 years of industry experience in mathematical modeling of biological systems.
Strong competency in coding and running modeling and simulation related software such as Matlab, NONMEM, Phoenix Winnonlin and R is required. Publication(s) applying modeling and simulation approaches to neurological diseases is preferred. Proficiency with systems modeling approaches such as differential equations, logic, stochastic, agent-based, mixed effects or other advanced mechanistic modeling approaches is essential. What Takeda can offer you: Comprehensive Healthcare: Medical, Dental, and Vision Financial Planning & Stability: 401(k) with company match and Annual Retirement Contribution Plan Health & Wellness programs including onsite flu shots and health screenings Generous time off for vacation and the option to purchase additional vacation days Community Outreach Programs and company match of charitable contributions Family Planning Support Flexible Work Paths Tuition reimbursement More about us: At Takeda, we are transforming patient care through the development of novel specialty medicals and best in class patient support programs.
Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work. Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. This position is currently classified as " hybrid" in accordance with Takeda's Hybrid and Remote Work policy. LOCATION: The role is based in Cambridge, MA or Fujisawa, Kanagawa Base Salary Range: $ 130,200-$186,000 may also be eligible for Short Term and Long-Term Incentive benefits.
Employees are eligible to participate in Medical, Dental, Vision, Life Insurance, 401(k), Charitable Contribution Match, Holidays, Personal Days & Vacation, Tuition Reimbursement Program and Paid Volunteer Time Off. The final salary offered for this position may take into account a number of factors including, but not limited to, location, skills, education, and experience. EEO Statement Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, interaction, interactionual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.
Locations Boston, MA Worker Type Employee Worker Sub-Type Regular Time Type Full time
be supported by several highly skilled data scientists, including those specializing in NLP. You will have available to you: a weekly study group, design review forums, code reviews, as well as access to annotators and several tasks to sharpen your skills. The ideal candidate has experience as the technical lead of NLP pipeline development.
This can be from academics, personal projects, competitions, open source, or professional work. Additionally, the applicant is expected to have a strong theoretical foundation in classical and modern NLP techniques. Highly motivated but less qualified or experienced candidates are absolutely encouraged to apply for either Junior or Intern positions.
Perks Flexible remote work, unlimited PTO, health/dental/vision plans, 401k, and equity option grants are available to full time data scientists at Verusen. Our Mission & You Verusen’s vision is to build an intelligent, connected supply chain.
Through years of well-meaning but haphazard information systems design, it is frequently the case that sharing information across the supply chain is incredibly difficult. Put simply, different parts of the supply chain refer to the same part in different and sometimes ambiguous ways. Our mission is not only to resolve these links, but to provide our customers with recommendations for those parts that are most at risk. Investors • Verusen is Venture
backed with investors including, Glasswing Ventures (Boston) • Flyover Capital (KC), Zetta Venture Partners (SF), Kubera VC (SF) and Engage • Ventures (ATL).
They are currently a Signature Company @ Georgia Tech’s Advanced • Technology Development Center (ATDC). Their partnerships include SAP, Accenture, and are a portfolio company of SAP. i O. What you will do: • Assist in the design of new experiments in our natural language processing pipelines. • Assist in the development of new NLP pipelines including data collection (including working with annotators), data extraction, data cleaning, exploratory data analysis, evaluative metric selection, baseline modeling, prototype modeling, error analysis, production modeling, and ongoing production support.
• With a focus on natural language processing and information retrieval. This person will be responsible for the end-to-end design, implementation, and monitoring of NLP pipelines. • The ideal candidate has significant experience as the technical lead of NLP pipeline development. This can be from academics, personal projects, competitions, open-source, or professional work. Additionally, the applicant is expected to have a strong theoretical foundation in classical and modern NLP techniques. Highly motivated but less qualified or experienced candidates are encouraged to apply for either Junior or Intern positions.
• As a Data Scientist in any position at Verusen, you will be supported by several highly skilled data scientists, including those specializing in NLP. You will have available to you: a weekly study group, design review forums, code reviews, as well as access to annotators and several tasks to sharpen your skills. As a member of a small team, your work will have a direct impact on both a large number of customers on our platform and on the future of a rapidly growing company. Responsibilities: • Creatively ideate on modifications to existing tasks and new tasks, while maintaining a focus on customer value and practical application.
• Experiment, build, maintain, and iterate on NLP pipelines. • Create, maintain, collaborate, and implement scientific and coding standards. Nice to Haves: • Python - including libraries like Tensorflow (or Py Torch), Sci-Kit learn, Pandas, and Numpy. • Experience creating production code including object-oriented programming principles. • Unit & integration testing • Experience with algorithmic design, complexity analysis, mathematic/scientific computing.
• Experience with supply chains. Qualifications • Masters Degree, Ph. D. preferred. Less traditional candidates will be seriously considered based on the strength of their portfolio. • Statistics: theoretical foundation in various common distributions, MAP/MLE, bayes, probability theory. • Familiarity with some statistical analysis software/library like Sci Py or SPSS, SAS, R, etc. • Natural Language Processing • Data engineering: SQL, Spark, Hadoop. • Various classifiers: Deep learning (including very modern approaches), forest-based classifiers, linear models, SVMs. Additional information Commitment to Diversity and Inclusion At Verusen, we are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants and teammates without regard to race, color, religion, interaction, national origin, age, physical and mental disability, interactionual orientation, gender identity and/or expression, status as a veteran and any other characteristic protected by applicable law.
We respect and seek to empower each individual and support a diverse culture, perspectives, skills, and experiences within our workforce. We believe that diversity and inclusion among our teammates are critical to our success, and we seek to recruit, develop and retain the most talented people from a dive candidate pool.
For more information about the Company, check us out at . "
most complex problems for a safer, healthier world. About the role: Laboratory Technician will be responsible for ensuring that timely and quality results are produced. Ensure that all tasks are performed within both the time restraints and the relevant analysis standards.
Highlight anomalies in results and sample type and sample behavior from running basic tests. Perform housekeeping duties as required. Calibrate equipment as required. Perform calculations as required when conducting analytical preparations. Prepare samples to be analyzed. Control consumable stock required for the tasks performed. Perform basic laboratory test. Create and maintain standards and reagents. Other
duties as assigned. Responsibilities About you: Proficient verbal and written communication skills. Excellent organizational skills and attention to detail.
Proficient computer skills, specifically Microsoft Office. Must be able to initiate corrective action without prompting and assist co-workers whenever necessary in order to meet deadlines. Must be able to effectively perform duties under pressures arising from large sample volumes and short turn-around times. Must be able to work independently with minimal supervision. Ability to use (or learn to use) Laboratory Information Management System. Excellent organizational skills and attention to detail. Follow all company operating
procedures, standards, policies, and training to ensure the safe and efficient operation of the site.
Play an active role in the ALS safety program by correcting or reporting unsafe acts and conditions that are observed during day to day operations to create a zero-injury work environment. Required Qualifications: AA is preferred. High school diploma/GED required. 1 - 3 years of laboratory experience is preferred. Physical Demands: The ability to stand for intervals of up to 8 hours while working; Able to speak and hear clearly while communicating with co-workers and managers; Dexterity in hands and fingers to operate equipment and handle glassware; Must have average vision and able to see to read reports and operate equipment; Hearing and speech to communicate in person and over the telephone.
Qualifications Working at ALS: Our people are our most valuable asset and drive our success at ALS. We are a diverse community of dedicated professionals united by our passion to make a difference in the world. We reward excellence and uphold our values in our work and how we treat each other. At ALS, you'll be supported to expand your skills and develop new ones so you can reach your full potential. We invest in our people with a range of programs and provide opportunities across the company, giving our people scope to grow diverse careers and develop as leaders.
We want everyone to have a safe, flexible and rewarding career that makes a positive impact on our people, the planet and the communities where we work. Our benefits include: Compensation Min$16.50-Max$18.50 Structured wage increases Comprehensive benefit package (including: medical, dental, and vision coverage, life and disability insurance, retirement plan with company match, employee assistance and wellness programs, access to company perks) Additional vacation days for years of service Business support for education or training after 9 months with the company Learning & development opportunities (unlimited access to e-learnings and more)About ALS: ALS is a global leader in scientific testing, providing comprehensive testing solutions to clients in more than 60 countries across a wide range of industries, including environment, food and beverage, mining, personal care, medical, healthcare and equipment reliability.
Using state-of-the-art technologies and innovative methodologies, our dedicated international teams deliver the highest-quality testing services and personalised solutions supported by local expertise.
We help our clients leverage the power of data-driven insights for a safer and healthier world. Everyone matters: ALS is proud to be an equal opportunity employer committed to achieving and maintaining a workforce which reflects and affirms the diversity of our society ALS is a VEVRAA Federal Contractor. EOE AA Minority, Female, Veteran, Individuals with Disabilities Click Here to view the EEO is the Law poster Click Here to view the FMLA Law poster Click Here to view the EPPA Law Poster Click Here to view the Pay Transparency Provision Click Here to view company E-Verify Participation Poster ALS also welcomes applications from people with all levels of ability.
Accommodation is available on request for candidates taking part in all aspects of the selection process.
hospitals. Sepsis mortality rate increases >6% every hour without effective antibiotic treatment. Yet, despite the life and death urgency, and healthcare cost impacts, current methodologies require 3 days to determine the correct antibiotic. Specific Diagnostics has developed a breakthrough solution to rapidly determine the effective antibiotic treatment for the bloodstream and other acute infections.
Used for bloodstream infection Specific’s solution provides results 2 days sooner than existing methods, saving patients suffering from a drug-resistant infection. We have been funded by nearly $30 M in non-dilutive government-sponsored research support and recently $17.5 M in venture
capital. This is an opportunity to join us at an inflection point in our commercial growth as we bring our first key product to market and with recognition from major customers fueling an expansion of our staff.
The Job This is the job for you if want to be where your ideas to be central to a world-changing and lifesaving product. Data science and analytics are at the core of our company we are seeking an exceptional talent to join our team. You will be a key contributor and critical to the success of the company. The main analysis tasks you are expected to contribute to are: • Analytical methods and statistical analysis for processing high-volume, temporal high-dimensional data streams
generated in real-time from our proprietary sensor technology. • The development of data-driven visualization tools for the explorative analysis of high-dimensional data.
• The application and development of suitable pre-processing, feature-selection, and dimensional reduction techniques to detect, measure and account for data artifacts. • The development and validation of applications for a medical instrument built under the guidance of a senior manager experienced in the application development discipline (so you’ll be learning the valuable skill of integrating your work into applications for medical diagnostic devices). • Algorithm development for decisions and measurements from multi-dimensional data streams.
• This is not the job for a numbers-only person. We want someone with a passion for and experience in the sciences that will lead you to look deeply into the sources of the data along with the scientists so that the data analysis is influenced by the science of our diagnostic technology and the science is influenced by the analysis. You You have a proven track record of successfully developing, validating, and deploying data analysis and analytical methods to solve challenging real-world applications. You are deeply familiar with a broad range of analytical models and are at the pulse of developments in the field.
Ideally, you have proven expertise in the analysis of Spatio-temporal data. You have strong domain knowledge in the field of statistical analysis and signal processing. You should have a track record of success in your education and projects and have these characteristics and skills: • MS degree in computer sciences, biomedical engineering, or related field and at least 5 years of interesting relevant experience. • Expert in R and proficient with C++ and Python. • Expertise in analytical methods and statistical analysis.
• Proficiency in SQL, as well as No SQL database technologies, is a plus. • Full fluency (verbal and written) of the English language is a must. /
most complex problems for a safer, healthier world. About the role: The primary purpose of this position is to manage the activities of staff members in the department and oversee the completion, review, and approval of assigned analyses and associated quality control requirements.
Ensure compliance with laboratory standards as stated in the laboratory Quality Systems Manual, corporate and laboratory SOPs and all certification requirements. Sustain an in-depth knowledge of all procedures performed in the department and insure these procedures comply with published methods, NELAC standards, state-specific requirements and good laboratory practices. Help management evaluate and maintain
appropriate staffing levels necessary to support operational needs. Insure that all quality control requirements associated with the department, including MDL/LOD/LOQ studies, SOP reviews, DOC requirements, and audit responses are completed in a timely manner.
Develop and implement new methods and technologies when mandated by changes in regulations or client needs. Complete performance evaluations and establish individual goals for department personnel on an annual basis. Uphold and enforce safety regulations as dictated and directed by corporate policy and the safety committee. Maintain a working knowledge of the laboratory LIMS system as it pertains to daily operation to monitor
laboratory workload and due dates in a continuous effort to improve the efficiency of the department; Direct and coordinate the activities of the department including the supervision of all personnel and capital resources available in order to successfully meet laboratory and client turnaround time requirements.
Review of department data and LIMS entries to ensure results are accurately reported; Responsibilities About you: Knowledgeable in EPA and SW-846 Organic Analysis and Preparation Methods, including all quality control requirement. Experienced in LCMS/MS applications for PFAS for method 537.1, 533, and 1633. Experience with supervision of personnel and workflow in a laboratory setting.
Familiarity with operation maintenance and data processing of Sctiex and Shimadzu LCMS/MS preferred; Strong industry specific computer skills including Star LIMS. Understanding of the principles and processes of the laboratory's quality system. Knowledge of laboratory safety policies. Possession of good organizational skills; detail oriented with the ability to multi-task. Possession of excellent problem solving capabilities. Ability to work irregularly scheduled hours including overtime and weekends if necessary Demonstrated strong maintenance and troubleshooting skills; Strong track record of method development including bringing on-line new methods, instruments and technologies; Possession of excellent verbal and written communication skills; Ability to work irregularly unscheduled hours including overtime and weekends as necessary.
Required Qualifications: 4 year college degree from an accredited educational institute in the chemical, environmental, biological, or physical sciences. 3 years of Organic analysis experience in an environmental laboratory. 1 year experience in a testing laboratory for PFAS and LCMS/MS preferred.
Physical Demands: The ability to speak and hear clearly while communicating with staff, management, and clients. Ability to sit and/or stand for 100% of an 8 hour day. Dexterity in hands and fingers to operate computer and other equipment. Average vision and ability to see to read reports and operate equipment. Hearing and speech to communicate in person and over the telephone. Qualifications Working at ALS: Our people are our most valuable asset and drive our success at ALS. We are a diverse community of dedicated professionals united by our passion to make a difference in the world.
We reward excellence and uphold our values in our work and how we treat each other. At ALS, you'll be supported to expand your skills and develop new ones so you can reach your full potential. We invest in our people with a range of programs and provide opportunities across the company, giving our people scope to grow diverse careers and develop as leaders. We want everyone to have a safe, flexible and rewarding career that makes a positive impact on our people, the planet and the communities where we work. Our benefits include: Compensation Min$23.91-Max$30.36 Structured wage increases Comprehensive benefit package (including: medical, dental, and vision coverage, life and disability insurance, retirement plan with company match, employee assistance and wellness programs, access to company perks) Additional vacation days for years of service Business support for education or training after 9 months with the company Learning & development opportunities (unlimited access to e-learnings and more)About ALS: ALS is a global leader in scientific testing, providing comprehensive testing solutions to clients in more than 60 countries across a wide range of industries, including environment, food and beverage, mining, personal care, medical, healthcare and equipment reliability.
Using state-of-the-art technologies and innovative methodologies, our dedicated international teams deliver the highest-quality testing services and personalised solutions supported by local expertise. We help our clients leverage the power of data-driven insights for a safer and healthier world. Everyone matters: ALS is proud to be an equal opportunity employer committed to achieving and maintaining a workforce which reflects and affirms the diversity of our society ALS is a VEVRAA Federal Contractor.
EOE AA Minority, Female, Veteran, Individuals with Disabilities Click Here to view the EEO is the Law poster Click Here to view the FMLA Law poster Click Here to view the EPPA Law Poster Click Here to view the Pay Transparency Provision Click Here to view company E-Verify Participation Poster ALS also welcomes applications from people with all levels of ability. Accommodation is available on request for candidates taking part in all aspects of the selection process.
most complex problems for a safer, healthier world. About the role: The primary purpose of this position is to receive and process samples from outside clients as well as field personnel. Will receive samples from outside clients and field service personnel and inspect for proper containers, temperatures, preservatives, etc.
Will accurately log samples into the laboratory LIMS system. Will be responsible for transporting samples to appropriate storage locations and disposing of expired samples Perform other duties as assigned and directed. Ensure compliance with assigned SOP's, QA manual and ALS Client Service Manual. Professional appearance and conduct to both ALS staff and clients.
Courier duites can be assigned. Other duties as assigned. Responsibilities About you: Desire to work in an administrative position in a laboratory setting.
Detail oriented - able to accurately interpret and transcribe information from a client chain of custody into the laboratory computer system. Good typing / data entry skills. Familiarity with chemical symbols and general scientific terminology. Have a demonstrated ability to communicate well in English, both verbal and written. Ability to multi-task and work as part of a team. Proven ability to learn new concepts quickly. Basic knowledge of EPA methodologies Current Driver's license with clean driving record. Ability to
operate company vehicle. Knows the region and able to read maps.
Able to take ownership for meeting goals and objectives; willing to be accountable for own decisions, and willing to give 100%. Look for new ways to accomplish objectives. English verbal and written communication skills with the ability to communicate with clients, staff and management. Multi-tasked, organized, detail oriented, and possesses problem solving capabilities; will have good time management capabilities. Self-motivated and self-directed; able to work independently. Required Qualifications: High School Diploma and some college level courses in a science curriculum are required.
A Bachelor of Science in Chemistry or a related field or previous laboratory experience is preferred. Possible travel to additonal labs in other areas. At less 2 years of experience required. Physical Demands: The ability to stand for intervals of up to 8 hours while working. Able to speak and hear clearly while communicating with co-workers and managers. Able to lift up to 50 lbs. on a consistent basis (may request and use a dolly for situations requiring heavy loads). Dexterity in hands and fingers to operate equipment and handle glassware. Must have average vision and able to see to read reports and operate equipment.
Hearing and speech to communicate in person and over the telephone. Qualifications Working at ALS: Our people are our most valuable asset and drive our success at ALS. We are a diverse community of dedicated professionals united by our passion to make a difference in the world. We reward excellence and uphold our values in our work and how we treat each other. At ALS, you'll be supported to expand your skills and develop new ones so you can reach your full potential. We invest in our people with a range of programs and provide opportunities across the company, giving our people scope to grow diverse careers and develop as leaders.
We want everyone to have a safe, flexible and rewarding career that makes a positive impact on our people, the planet and the communities where we work. Our benefits include: Structured wage increases Comprehensive benefit package (including: medical, dental, and vision coverage, life and disability insurance, retirement plan with company match, employee assistance and wellness programs, access to company perks) Additional vacation days for years of service Business support for education or training after 9 months with the company Learning & development opportunities (unlimited access to e-learnings and more)About ALS: ALS is a global leader in scientific testing, providing comprehensive testing solutions to clients in more than 60 countries across a wide range of industries, including environment, food and beverage, mining, personal care, medical, healthcare and equipment reliability.
Using state-of-the-art technologies and innovative methodologies, our dedicated international teams deliver the highest-quality testing services and personalised solutions supported by local expertise. We help our clients leverage the power of data-driven insights for a safer and healthier world.
Everyone matters: ALS is proud to be an equal opportunity employer committed to achieving and maintaining a workforce which reflects and affirms the diversity of our society ALS is a VEVRAA Federal Contractor. EOE AA Minority, Female, Veteran, Individuals with Disabilities Click Here to view the EEO is the Law poster Click Here to view the FMLA Law poster Click Here to view the EPPA Law Poster Click Here to view the Pay Transparency Provision Click Here to view company E-Verify Participation Poster ALS also welcomes applications from people with all levels of ability.
Accommodation is available on request for candidates taking part in all aspects of the selection process.
research and development to create a cutting-edge in vitro diagnostic system. Experience in product development for medical diagnostics is preferred. Ideally, you have proven expertise in planning and executing laboratory experiments, preparing, and giving presentations, data preparation and acquisition, and data interpretation.
Domain knowledge in protocols, execution of clinical studies, and experience working within regulatory guidelines is a definite plus. The job requires in-depth knowledge and proficiency in standard microbiological methods such as dilution and enumeration of microorganisms, stocking frozen strains, isolation, and identification of pathogenic microorganisms, preparation
and sterilization of culture media, aseptic techniques, components of culture media, and impact on growth. You must be able to work in compliance with FDA and ISO guidelines in the regulated IVD arena.
Key responsibilities include: • Working independently and as a member of a cross-functional team to support microbiology research and development. • Preparing data decks and giving presentations for various studies. • Working as a member of the development team executing analytical and research studies. • Providing team members with technical guidance and training, as well as identifying resources needed to meet or exceed project goals. • Authoring and reviewing protocols, reports, SOPs,
work instructions, and other product-related documents.
You Creating new-to-the-world, impactful products, requires passion, smarts, strength, persistence, and hard work. You should be able to solve difficult problems and get big things done. You will be self-motivated, highly organized, and flexible. Ability to independently manage a project is needed and you must be able to adapt to shifting priorities. You should be excited by the prospect of working in a dynamic, entrepreneurial environment. We are adding only the most exceptional talent to our outstanding team of engineers and scientists. You should have a track record of success in your education and projects, along with the following characteristics and skills: • Ph D in Microbiology or similar discipline with 1+ years of industry microbiology and/or medical diagnostics, or M.
S. in equivalent major with 4+ years in microbiology and/or medical diagnostics. • Strong research background. Exceptional skills in preparing presentations and analyzing data. • Experience working with a team of microbiologists. Previous track record of collaboration within a fast-paced environment a plus. • Proven proficiency in data analysis, research design, troubleshooting, and evaluation of new technologies and procedures.
• Experience in the development and validation of clinical diagnostic/susceptibility assays for infectious disease. • Teamwork experience, start-up experience and knowledge of AST is a plus, but not a pre-requisite. • Clinical Microbiology Laboratory experience is a plus. • Experience working with multidrug-resistant bacteria and/or Mycobacterium Tuberculosis is preferred. • A team player that works well can independently and as part of a team. • Ready for a fast-paced biotech start-up. Job Type: Full-time
histology assays. • optimizing whole-tissue staining, • clearing and imaging protocols, • generating novel analysis routines, and • summarizing results for publication or reporting The selected candidate will report directly to the scientific leadership team and work with a diverse group of researchers across multiple disciplines.
The Scientist will lead research efforts on various projects, designing experiments, generating timelines, and executing experiments and data analyses in a timely manner. Candidates must have a demonstrated record of scientific productivity, creativity and rigor. Strong organizational and communication skills will be critical for success in the role. While pre-clinical
Neuroscience is a primary focus of our research currently, we welcome candidates from all biological disciplines. If you are interested in developing state-of-the-art assays, enjoy creating new tools, and would like to work in a team-oriented environment, please apply.
We are located in the research park next to UC Irvine. Irvine is in Orange County, California, where a growing hub for biotech startups is situated and it is close to amazing food, biking/hiking trails and beaches. This position is ideal for a recent Ph. D. graduate interested in making an impact on scientific knowledge by contributing to development of exciting new tools to expediate and enrich the way scientific discoveries
are made across multiple disciplines. • Ph. D.
degree in Neuroscience, Immunology, Oncology or other biology discipline • Extensive immunostaining experience, ideally with tissue clearing methods • Demonstrated experience in quantitative image analysis • Computational skills, including experience with Python or bash scripts • Proven ability to operate in a collaborative team environment • Strong written and verbal communication skills Responsibilities: • Design, perform, analyze and rigorously document experiments • Lead research projects and coordinate activities of research associates • Present data to research teams, management and communicate findings in publications, posters and conference presentations • Manage collaborations with industry and academic partners • Assist with writing manuscripts, reports, grant applications and patent filings
We provide exceptional opportunities for those who have the entrepreneurial spirit, enjoy developing novel technology platforms and products, and aspire to grow together with the company. Description: We are seeking a Ph D level scientist with a passion for innovation to augment the capability of our novel Biomarker detection and quantitation.
You will be working in a fast-paced environment, on multiple projects, and will be a part of a rapidly growing company to make a big impact in life science research and clinical diagnostics. Key Responsibilities • Design and execute experiments for new biomarker detection. • Examine the impacts of multiple variables on assay performance. • Proactively
identify opportunities for product and process improvement. • Develop and document technology/product requirements, protocols, work instructions. Required Knowledge/Skills, Education, and Experience • Ph.
D degree in biochemistry, molecular biology or a related discipline; or BS/MS with substantial relevant experience. • Hands on experience running ELISA, q PCR or similar, as well as experience generating, analyzing, and reviewing data from those assays required. • Self-motivation with a positive “can do” attitude, attention to details and ability to manage complex projects are critical. • Knowledge in emerging reagent and immunoassay technologies desirable. • Knowledge in biomarker discovery,
assay prototyping, performance optimization, and control system design preferred.
• Data management skills highly beneficial. • Strong communication skills to work within a multidisciplinary team environment required.
Injectable Aesthetics, Dermo-cosmetics, and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals.
Because we understand that the skin we're in shapes our lives, we are advancing dermatology for every skin story. We look for people who focus on getting results, embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all, they must be passionate about doing something meaningful for consumers, patients, and the healthcare
professionals we serve every day. We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee.
At Galderma, we actively give our teams reasons to believe in our bold ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact. Job Title: Field Access Director, Southeast Location: Remote, Southeast, USJob Description The Field Access Director will lead a regional team of Field
Access Managers in assisting accounts in gaining access to Galderma's biologic treatment.
The role is in Galderma's Prescription Business Unit and will provide reimbursement assistance, education, and general access support to patients with prurigo nodularis and atopic dermatitis. The role will have a specified geography and partner closely with key stakeholders within the US cross functional teams as well as external partners, and directly reports to the Senior Director of National Field Reimbursement. As the regional leader of the Field Access Management (FAM) team, you will manage and develop the performance of the FAMs in a specific area, support the execution of strategic and tactical initiatives; monitor and manage the team's compliance with the program's business rules, serve as an escalation point for field-based access issues, work collaboratively with Sales Directors, Market Access and Patient Services colleagues.
Work directly and collaboratively with the Prescription Business Unit Director team to: Assist in the development, training and on-boarding of the FAM team Support the evolution of the FAM team as the role develops, patient and the business needs and market evolve Monitor appropriate metrics to measure performance, communicate those metrics to internal stakeholders Manage the on-going educational needs, assist in the on-boarding and training of the FAM team Key Skills, Abilities and Competencies Ability to build and lead a team in identifying access solutions and determine the appropriate plan of action for patient access Manage team metrics, budget and performance Experience working with patients on specialty products Demonstrate an expertise level on access challenges through their experience working on similar role in the specialty space Ability to lead internally to achieve common goals by collaborating Market Access, Legal, Compliance, Commercial functions Assist in the development of impactful educational pre-launch and launch needs Partner with teams that will be responsible for executing on access tactics and materials across all patient channels Collaborate with sales, training and other stakeholders as appropriate in development and execution of training plan for patient access materials Identify emerging trends with access challenges within all channels and apply insight to development of solutions that support a positive patient journey experience Accountable for cross-functional communication internally and externally among a diverse set of customers Minimum Requirements: Bachelor's degree in relevant field required.
5+ years of experience in the medical industry in a reimbursement/access role Demonstrated success managing a team Strong ability to translate access issues into appropriate talking points for patient audience Cross-functional experience required, proven track record of collaboration and coordination Exceptional communication and presentation skills: ability to articulate a point of view succinctly and effectively to leadership and external customers Comprehensive analytical/strategic thinking skills; demonstrated ability to use data in fact-based decision-making (data to insights, to action).
Ability and confidence to work effectively and with a sense of urgency Adaptability, resilience and tenacity and ability to quickly pivot Proficient in English, MS Office; especially Word, Excel, and Power Point Availability to travel >30% time Other Requirements/Qualifications: Experience in biopharma Patient Services or Market Access preferred Experience with biologics and specialty products preferred. Experience in dermatology/immunology preferred Launch experience preferred What we offer in return You will be working for an organization that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.
You will also have access to a range of company benefits, including a competitive wage with shift differential, annual bonus opportunities and career advancement and cross-training. Next Steps If your application is successful and your profile is a match, we will invite you for a first virtual conversation with the recruiter. The next step is a virtual conversation with the hiring manager The final step is a panel conversation with the extended team Our people make a difference At Galderma, you'll work with people who are like you.
And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do. Employer's Rights: This job description does not list all the duties of the job. You may be asked by your supervisors or managers to perform other duties. You will be evaluated in part based on your performance of the tasks listed in this job description.
The employer has the right to revise this job description at any time. This job description is not an employment contract, and either you or the employer may terminate employment at any time, for any reason. In addition, reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.