funding. The aim of the program is to nurture a diverse group of promising scholars and to increase the critical mass of scholars with interests in formal theory and quantitative methods at Princeton. Interested applicants must apply online at www. princeton.
edu/acad-positions/position/31821 and submit a CV, cover letter, writing sample, transcript and the names and contact information of three references. Ph. D. is required. The cover letter should describe how applicants might engage in collaborative research projects with Princeton Politics faculty members. Unofficial transcripts are sufficient and may be uploaded with the application. Applicants who are unable to upload unofficial
transcripts may send official transcripts to F/Q Postdoc Search, Department of Politics, 001 Fisher Hall, Princeton University, Princeton, NJ 08544. We will begin reviewing applications on February 15, 2024.
This position is subject to the University's background check policy. Princeton University is an Equal Opportunity/Affirmative Action Employer and all qualified applicants will receive consideration for employment without regard to age, race, color, religion, interaction, interactionual orientation, gender identity or expression, national origin, disability status, protected veteran status, or any other characteristic protected by law. EEO IS THE LAW recblid 5vwvx0kp3aawnc2phjbgwx2jwkyds3 PDN-9ad3d36de-c561bc7f7470
and your contributions make a difference for patients and families. Join us as we build on our promise to advance pediatric care-and your career. CHOP's Commitment to Diversity, Equity, and Inclusion CHOP is committed to building an inclusive culture where employees feel a sense of belonging, connection, and community within their workplace.
We are a team dedicated to fostering an environment that allows for all to be their authentic selves. We are focused on attracting, cultivating, and retaining diverse talent who can help us deliver on our mission to be a world leader in the advancement of healthcare for children. We strongly encourage all candidates of diverse backgrounds and lived
experiences to apply. A Brief Overview This role is reserved for positions impacted by the federal Fair Labor Standards Act (FLSA) or the local equivalent. Please reach out to HR with further questions.
This role is an advanced independent researcher that plans, coordinates and executes complex research projects. Works with the Principal Investigator. Participates in and assists in the planning and coordination of research projects, is independent and responsible for a specific aspect of the one or more research projects. Assists in determining the direction of the project. Prepares and writes manuscripts and research proposals, performs data management and quantitative analyses, collaborates
in development of innovative research and educational programs, and serves as an educational resource for the laboratory and the Institution.
What you will do Assists faculty in the conduct of research of significant value in the basic and/or translational science area Functions with a high level of independence in the development and execution of research projects Plans, conducts, and manages research projects within the federal, institutional regulations and policies Collaborates with researchers, external agencies and institutions to develop cooperative research initiatives Trains technical staff, students, fellows, and physicians in lab procedures Reviews manuscripts for peer-reviewed journals Assist in composing/developing applications for grants, contracts, and research funding proposals.
Responsible for appropriate use of research funds May supervise students or other research staff as assigned. Education Qualifications Bachelor's Degree Required Master's Degree Preferred Doctorate Preferred Experience Qualifications At least eight (8) years of directly relevant post grad scientific lab experience Required At least ten (10) years of directly relevant post grad scientific lab experience Preferred Successful completion of a Post Doc Fellowship Preferred Skills and Abilities Expert knowledge in the use of a wide variety of lab techniques, research equipment and research related software Excellent verbal and written communications skills Excellent organizational skills Excellent critical thinking / problem-solving skills Excellent analytical skills Strong interpersonal skills Solid leadership skills To carry out its mission, CHOP is committed to supporting the health of our patients, families, workforce, and global community.
As a condition of employment, CHOP employees who work in patient care buildings or who have patient facing responsibilities must be fully vaccinated against COVID-19 and receive an annual influenza vaccine.
Learn more. Employees may request exemptions for valid religious and medical reasons. Start dates may be delayed until candidates are immunized or exemption requests are reviewed. EEO / VEVRAA Federal Contractor Tobacco Statement
that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide. Therefore, only applications that are submitted in English will be considered. At Sanofi diversity and inclusion is foundational to how we operate and is embedded in our Core Values.
We respect the diversity of our people, their backgrounds and experiences. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our employees, patients and customers. We are looking for: Research Scientist - VIE Contract (W/M) Target start date: 01/01/2024 Responsibilities:
Working as part of an international team for antibody discovery and characterization against several pathogenic targets Bibliography analysis on new technical development for antibody discovery programs Identification and implementation of novel approaches pertinent to state-of-the-art fields in immunology, antibody discovery, single cell approaches, Next Generation Sequencing (NGS) to support innovative, rapid, and disruptive methods and technologies Set up and perform experimentation with new technical developments and formal and informal presentation of results obtained in platform, scrum reviews, and scrum grand reviews Supporting the identification and acquisition of technologies and equipment
Work independently utilizing various experimental techniques, with a willingness to implement innovative technologies and protocols Understand goals and identify own role in achieving them, meeting key deadlines that are set Document all work appropriately in electronic lab notebooks and perform laboratory support activities such as maintaining equipment and ordering lab supplies Work with contract research organizations (CROs) as needed Requirements: Ph.
D. or Master's degree + experience in Immunology/Virology or similar with previous experience in antibody discovery, immunology, and/or molecular biology or similar field Ideally, first professional experience as a research or engineer in the above-mentioned subject areas Hands-on experience with flow cytometry and/or cell sorting, including experience with the associated software packages (e.
g. Flow Jo) Strong experience in the theory and performance of immunology and molecular biology methods Experience in analytics approaches and use of software Proficient with Microsoft Office Suite Fluent in English language, French will be a plus point Excellent interpersonal skills, communication, and a collaborative attitude to work in multidisciplinary teams Ability to independently exercise judgment in daily duties, plan and execute experiments in a timely manner is critical Highly motivated, reliable, and well-organized individual Ability to learn recent technologies and concepts and apply them appropriately with supervision Experience with protein biochemistry and/or protein characterization (surface plasmon resonance (SPR), biolayer interferometry (Octet), ELISA) a plus Experience in single cell genomics approaches, NGS, antibody identification, and generation a plus Familiar with common software and tools for data analysis in the fields of immunology and/or antibody discovery will be a plus At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values.
We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all. i Move, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.
PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship. PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide. Therefore, only applications that are submitted in English will be considered. At Sanofi diversity and inclusion is foundational to how we operate and is embedded in our Core Values. We respect the diversity of our people, their backgrounds and experiences.
We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our employees, patients and customers. We are looking for: Research Scientist - VIE Contract (W/M) Target start date: 01/01/2024 Responsibilities: Working as part of an international team for antibody discovery and characterization against several pathogenic targets Bibliography analysis on new technical development for antibody discovery programs Identification and implementation of novel approaches pertinent to state-of-the-art fields in immunology, antibody discovery, single cell approaches, Next Generation Sequencing (NGS) to support innovative, rapid, and disruptive methods and technologies Set up and perform experimentation with new technical developments and formal and informal presentation of results obtained in platform, scrum reviews, and scrum grand reviews Supporting the identification and acquisition of technologies and equipment Work independently utilizing various experimental techniques, with a willingness to implement innovative technologies and protocols Understand goals and identify own role in achieving them, meeting key deadlines that are set Document all work appropriately in electronic lab notebooks and perform laboratory support activities such as maintaining equipment and ordering lab supplies Work with contract research organizations (CROs) as needed Requirements: Ph.
D. or Master's degree + experience in Immunology/Virology or similar with previous experience in antibody discovery, immunology, and/or molecular biology or similar field Ideally, first professional experience as a research or engineer in the above-mentioned subject areas Hands-on experience with flow cytometry and/or cell sorting, including experience with the associated software packages (e.
g. Flow Jo) Strong experience in the theory and performance of immunology and molecular biology methods Experience in analytics approaches and use of software Proficient with Microsoft Office Suite Fluent in English language, French will be a plus point Excellent interpersonal skills, communication, and a collaborative attitude to work in multidisciplinary teams Ability to independently exercise judgment in daily duties, plan and execute experiments in a timely manner is critical Highly motivated, reliable, and well-organized individual Ability to learn recent technologies and concepts and apply them appropriately with supervision Experience with protein biochemistry and/or protein characterization (surface plasmon resonance (SPR), biolayer interferometry (Octet), ELISA) a plus Experience in single cell genomics approaches, NGS, antibody identification, and generation a plus Familiar with common software and tools for data analysis in the fields of immunology and/or antibody discovery will be a plus At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values.
We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all. PDN-991f3510-f227-4342-ba88-226547827b77
and maintenance of subjects in clinical trials, and by collecting, recording, and maintaining source and sponsor documentation. Primary Responsibilities: • Understand thoroughly all assigned studies through reading protocols, attending investigator meetings and start-up meetings, and coordinating with Principal Investigator• Adhere strictly to the study protocol; obtain exemptions when necessary/appropriate• Communicate protocol issues to CRO and/or Sponsor, Site Administrator, Director, Principal or Sub-Investigator• Articulate all pertinent issues to the Pl or document by email/letter or during meetings• Collect initial psychiatric and medical information by interviewing patients and by accessing
other appropriate sources• Ensure a flow of communication including telephone conferences between patient, study staff, referral sources, Sponsor and/or CRO, Monitor(s), Auditors and any marketing groups hired by the Sponsor• Utilize various psychiatric rating scales and maintaining interrater reliability with other clinicians at K2 Medical Research• Perform clinical tasks including, but not limited to, vital signs, height and weight, ECG, phlebotomy, specimen packaging• Maintain timely K2 Medical Research source documentation as well as sponsor required information.
• Dispense and maintain accurate records of study medication• Educate patients and family regarding their particular study
and clinical drug trials in general. • Complete all monitor and sponsor queries in a timely manner• Provide appropriate community resource referrals to patients, caretakers, and family at conclusion of patient's participation in study Knowledge, Skills, and Abilities: • Outstanding verbal and written communication skills• Excellent interpersonal and customer services skills • Strong time management and organizational skills In depth knowledge of industry regulations • Proven ability to and foster mentoring relationships• Ability to create momentum and foster organizational change Qualifications: • HS Diploma or GED Transcript required.
Bachelor's degree strongly preferred.
• Prior experience in a clinical environment preferred. Experience in clinical research is ideal. • LPN, RN, or other medical licensure or certification preferred. • Strong working knowledge of GCP and FDA guidelines• Knowledge of medical terminology• BLS Healthcare Provider required • Bilingual Preferred• Applicants that do not meet 100% of the above qualifications but who have a combination of related education and applicable experience may be considered upon approval
trials, and by collecting, recording, and maintaining source and sponsor documentation. Primary Responsibilities: • Understand thoroughly all assigned studies through reading protocols, attending investigator meetings and start-up meetings, and coordinating with Principal Investigator• Assist the Site Director and Project Management team on projects as needed• Adhere strictly to the study protocol; obtain exemptions when necessary/appropriate• Communicate protocol issues to CRO and/or Sponsor, Site Administrator, Director, Principal or Sub-Investigator• Articulate all pertinent issues to the Pl or document by email/letter or during meetings• Collect initial psychiatric and medical information
by interviewing patients and by accessing other appropriate sources• Ensure a flow of communication including telephone conferences between patient, study staff, referral sources, Sponsor and/or CRO, Monitor{s), Auditors and any marketing groups hired by the Sponsor• Utilize various psychiatric rating scales and maintaining interrater reliability with other clinicians at Compass Research• Perform clinical tasks including, but not limited to, vital signs, height and weight, ECG, phlebotomy, specimen packaging• Maintain timely K2 Medical Research source documentation as well as sponsor required information.
• Dispense and maintain accurate records of study medication• Educate patients and
family regarding their study and clinical drug trials in general.
• Complete all monitor and sponsor queries in a timely manner• Provide appropriate community resource referrals to patients, caretakers, and family at conclusion of patient's participation in study Knowledge, Skills, and Abilities: • Outstanding verbal and written communication skills• Excellent interpersonal and customer services skills • Strong time management and organizational skills In depth knowledge of industry regulations • Proven ability to and foster mentoring relationships• Ability to create momentum and foster organizational change Qualifications: • HS Diploma or GED Transcript required.
Bachelor's degree strongly preferred. • Prior experience in a clinical environment preferred. Experience in clinical research is ideal. • LPN, RN, or other medical licensure or certification preferred. • Applicants that don't meet 100% of the above qualifications but who have a combination of related education, applicable experience, demonstrated capability, and a genuine passion for success in this position may also be consider.
to day activities of research protocols for the Epidemiology program and supporting all research efforts of the program. Daily activities include screening, enrollment, and monitoring of research participants as well as ensuring accurate data collection, documentation, organization and safety of research participants.
This individual should have excellent communication skills since study participants may be recruited in person, via phone, or email. Research coordinator will also be responsible for completing all relevant study documents, maintaining research charts, providing study updates, and completing study progress reports. Job Duties Interviews, screen and recruits patients for
study; explains process and procedures to educate participant regarding the research study. Ensure research protocol objectives are being met and research activities meet institutional and regulatory standards.
Collects patient information; processes documents and enters information into a database. May collect, process, ship, and maintain paperwork for specimens according to procedures outlined in study protocol. Maintains records and regulatory documents for research studies. Organizes study research documents following specific protocol guidelines. May correspond with patients throughout study. Work in a team environment with faculty and other staff members to ensure protocol objectives
are being met. Schedule study meetings and conference calls. Prepare study meeting agendas, participate in meetings, and track meeting minutes/notes.
Performs other job duties as assigned. Minimum Qualifications High School diploma or GED. Three years of relevant experience. Preferred Qualifications Bachelor's degree in Public Health or related. Experience working with children. Bilingual in Spanish Clinical Research experience. Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer. 18013
disciplines. This role recognizes critical and significant findings, reports test results, and maintains records of patient tests. Also, recognizes technical, instrumental, or physiological problems that could adversely affect tests or results, resolves, and documents.
Performs calibration and maintenance of laboratory instruments. Adheres to quality control protocols to ensure accuracy of results. Monitors the accuracy and precision of all laboratory tests personally performed. Actively participates in continuing education programs. Communicates technical and general information to manager and medical staff. Projects an image of professionalism in communication, appearance and conduct.
Supports the laboratory mission. Participates in the continuous quality improvement process. Maintains a working knowledge of departmental standard operating procedures.
This knowledge may include the use of specialized instrumentation, quality control requirements, and preventative maintenance. Performs other duties as assigned. Education and Experience Required: Baccalaureate Degree in medical technology or related science. License Required: Must meet and maintain current State of California licensure requirements for one of the following: Clinical Laboratory Scientist or one of the following Limited Clinical Laboratory Scientist Clinical Chemist Scientist (work limited to Chemistry
only) Clinical Hematologist Scientist (work limited to Hematology only) Clinical Immunohematologist Scientist (work limited to Blood Bank only) Clinical Microbiologist Scientist (work limited to Microbiology only) Public Health Microbiologist Certification (work limited to Microbiology & Immunology/Serology) About Hoag Hoag is a nonprofit, regional healthcare delivery system in Orange County, California.
Delivering world-class, comprehensive, personalized care, Hoag consists of 1,800 top physicians, 15 urgent care facilities, 10 health and wellness centers, and two award-winning hospitals. Hoag offers a comprehensive blend of health care services that includes seven institutes providing specialized services in the following areas: cancer , digestive health , heart and vascular , neurosciences , spine , women's health , and orthopedics through Hoag's affiliate, Hoag Orthopedic Institute , which consists of an orthopedic hospital and four ambulatory surgical centers.
Hoag is the highest-ranked hospital in Orange County by U. S. News & World Report and the only OC hospital ranked in the Top 10 in California, as well as a designated Magnet® hospital by the American Nurses Credentialing Center (ANCC). For more information about Hoag careers, visit careers. hoag. org.
- Influenced product decision making in past research projects. - Worked previously in the tech industry · Performance Indicators - Quality of work Top 3 Hard Skills Required - 5-7 years of experience 1. Strong research skillset – breadth of methodologies (qual and quant research) 2.
Strong report generation 3. Strong data analysis" " Summary: In this role, you will be part of the team responsible for Power Point user experience research. You will build and execute impactful research plan(s) that provide the broad market views and deep customer insights needed to impact UX decisions. You will derive insights from quantitative and qualitative data, complementing other research
that you will conduct on your own or in partnership with other researchers. Responsibilities: Planning and executing qualitative or mixed methods research studies and experiments to discover and apply insights to the design of Office products, with a primary focus on Power Point.
Analyzing and synthesizing data, sensemaking across multiple data sources, prioritizing issues, and tracking impact of research. Skills and Experience (required): An advanced degree in an Engineering, Social Science, or other data- or research-centric field. Experience with qualitative research methods, insight synthesis, and insight report generation. Industry experience advocating for the customer and effectively
partnering with development teams to improve the user experience based on research results or customer feedback.
Passion for fundamentally translating ideas, needs, and requests into researchable questions in a rigorous and valid way. Strong project management, organization, and planning skills with an attention to detail. Highly polished written and verbal communication and presentation skills, including influencing teams making data-driven decisions. Skills and Experience (Desirable): An advanced degree in Human Computer Interaction, Human Factors, or related field. Experience and demonstrated skill with qualitative usability methods, including observing, understanding, and synthesizing human behavior into insights, and driving the voice of the customer in product development.
" " Typical Day in the Role · Purpose of the Team - This is a research team that cover a variety of MSFT experiences – primarily focused on MSFT Power Point. This team does mixed methods of research across Office experiences that are focused on storytelling and AI. · Key projects - See JD · Typical task breakdown and operating rhythm - - Meeting with stakeholders to scope out research project. - Conducting and gathering data for the project - Analyzing data – creating reports and outputs - Activating research and sharing with stakeholders
guidance and assistance for dissemination of scholarly work. Overview Preferred Qualifications Role Purpose Develops the health services research program. Facilitates and independently conducts academic/clinical research, supports research utilization in nursing/clinical practice and develops an ongoing strategic plan for academic/clinical research.
Responsibilities Conducts interdisciplinary research and evidence-based practice projects that support the organization? s priorities for improving patient and/or care delivery outcomes. Serves in a consultative role for patient care services staff in the development and completion of interdisciplinary research and evidence based practice
projects and scholarly activities. Collaborates with patient care services clinicians, including physician partners, to evaluate and implement best practices for clinical care, patient care delivery models, education and use of technology.
Mentors nursing and allied health professionals in developing presentations, posters and written articles or abstracts. Presents original research and evidence based practice at regional and national conferences with poster or podium presentations and submits for publication in peer-review journals. Minimum Requirements Education Doctorate - Nursing/Healthcare related Experience5-10 years Supervisor Experience No Experience Licenses & Certifications
Cert/Lic in Area of Expertise Benefits and Legal Statement BJC Total Rewards At BJC we’re committed to providing you and your family with benefits and resources to help you manage your physical, emotional, social and financial well-being.
Comprehensive medical, dental, vison, life insurance, and legal services available first day of the month after hire date Disability insurance paid for by BJCPension Plan/403(b) Plan funded by BJC401(k) plan with BJC match Tuition Assistance available on first day BJC Institute for Learning and Development Health Care and Dependent Care Flexible Spending Accounts Paid Time Off benefit combines vacation, sick days, holidays and personal time Adoption assistance To learn more, go to /Benefits Not all benefits apply to all jobs The above information on this description has been designed to indicate the general nature and level of work performed by employees in this position.
It is not designed to contain or be interpreted as an exhaustive list of all responsibilities, duties and qualifications required of employees assigned to this job. Equal Opportunity Employer For more details: jobs-search. org/finance_missouri-r782067/research-scientist-phd-rn-st-louis_i1950754367
and Companionship Enriching Life. Elanco's promise to employees: Together, we foster an inclusive culture where everyone can make a difference, encouraging ownership, growth and well-being. The Senior Research Scientist is responsible for the development, qualification/validation, and use of analytical, bioanalytical and characterization methods in support of Elanco’s Food and Companion Animal Vaccine product development.
This role is expected to benchmark the Animal Health industry and drive the change to put Elanco at the Innovation forefront. This lead scientist will additionally be charged with creating a culture of intellectual curiosity that implements best practices of Qb D and
drives the analytical development for successful release of vaccine. Functions, Duties, Tasks: Lead development for the vaccines analytical control strategy. Benchmark against the industrystandards and partner with Regulatory and Quality to align and define the registration strategy.
Establish the analytical capability that creates a strategic advantage against industry peers. Partner with Global Vaccine Strategy (R&D, QC, Regulatory and Manufacturing) Transfer of methods to Quality Control, or third-party personnel. Development and verification/qualification/validation of analytical methods to support in- process, release, characterization analysis, and stability testing of antigen
ingredient and final vaccine. Write, review, and/or approve high quality technical reports, SOPs, analytical methods, global regulatory submissions, and responses to questions.
Ensure work and team activities are aligned with all relevant development quality, regulatory, HSE, GLP, and GMP requirements. Minimum Qualification (education, experience and/or training, required certifications): Ph. D. in analytical, biophysical, biochemistry, molecular/cell biology, or related field; alternatively, skills commensurate with a Ph D scientist. Minimum 3-8 years’ experience in relevant/applicable field. Experience with knowledge of one or more of the following, as appropriate: separation sciences, immunochemistry, biophysical/biochemical characterization, molecular biology, and bioanalytical sciences.
Problem solving skills including strategic thinking and decision-making. Effective oral and written communication skills. Must be able to work productively in an interdisciplinary team environment. Ability to work successfully in international or multi-cultural settings. Ability to handle multiple priorities and deal with ambiguity. Additional Preferences: Experience with assay development in the Animal Health industry is highly desired. Experience with the vaccine development process, including knowledge of regulatory compliance issues.
Fundamental knowledge of c GMP/GLP/USDA compliance requirements. Experience with partnering and leading teams remotely. Other Information: Position will require up to 25% travel. Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, interactionual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
and practices that foster diversity in ideas and in the people across the organization, as well as to ensure ORNL is recognized as a workplace of choice. These elements are critical for enabling the execution of ORNL’s broader mission to accelerate scientific discoveries and their translation into energy, environment, and security solutions for the nation.
We are seeking a Postdoctoral Research Associate who will support the Plant-Microbe Interfaces (PMI) Scientific Focus Area (pmi. ornl. gov), Molecular and Cellular Imaging Group in the Biosciences Division, Biological and Environmental System Sciences Directorate (BESSED) at Oak Ridge National Laboratory (ORNL). A major focus of the
PMI project is to gain a deeper understanding of the diversity and functioning of mutually beneficial interactions between plants and microbes. Plants are host to a diverse microbial community that resides within and on plant tissues.
A key research emphasis within the project is on understanding the metabolic and molecular mechanisms underlying plant-microbe and microbe-microbe interactions in these complex ecosystems. To support this effort, an interdisciplinary group focuses on microbial isolation from rhizosphere samples, physiological characterization, image analysis, comparative genomics, plant-microbe model system development and experimentation for understanding physical and molecular
mechanisms of microbe-microbe and plant-microbe interactions that influence microbial community structure and host plant physiology and phenotypes.
A major thrust in this work is to visualize and quantify the dynamic evolution of the host, its associated microbial communities, and the local physical and chemical environment in which these complex changes occur. The post-doctoral research associate will focus on continuing the development of microfluidic, 3D-printed and rhizotron platforms that will enable real-time imaging and chemical sampling of developing multi-kingdom systems. Work will be conducted within a highly interdisciplinary environment to create engineered habitats that enable high throughput phenotyping and advanced multimodal imaging of biological systems and soft materials.
Your work will combine micro- and nanofabrication, microfluidic assembly, imaging, and cell biology. Major Duties/Responsibilities: Conduct collaborative scientific research using constructed microbial communities and monitor host and community development using optical microscopy and quantitative image analysis. Lead and contribute to the preparation of scientific manuscripts. Present research findings at national and international scientific meetings.
Work independently to support interdisciplinary research efforts within the Plant-Microbe Interfaces project. Deliver ORNL’s mission by aligning behaviors, priorities, and interactions with our core values of Impact, Integrity, Teamwork, Safety, and Service. Promote diversity, equity, inclusion, and accessibility by fostering a respectful workplace – in how we treat one another, work together, and measure success. Basic Qualifications: A Ph D in Microbiology, Molecular Biology, Biochemistry, Chemical Engineering, Bioengineering, or a related field completed within the last 5 years Demonstrated expertise working with a breadth of micro- and nanofabrication techniques and/or 3D printing technologies to shape inorganic materials and fluidic platforms to effectively interface with and control biological systems.
Preferred Qualifications: Demonstrated expertise in one or more of the following areas is desirable: microbiology, plant-microbe interactions, microfluidics and microfabrication, image analysis. Experience with fabrication techniques that include photolithography, electron beam lithography, reactive ion etching, physical and chemical vapor deposition and atomic layer deposition processes.
Experience with optical microscopy, scanning probe microscopy, and associated image analysis techniques. Demonstrated experience working with biological systems in one or more of the following areas: microbial physiology, micro- and molecular biology, plant-microbe interactions, plant physiology, fungal biology, and/or mammalian cell biology. Excellent written and oral communication skills Motivated self-starter with the ability to work independently and to participate creatively in collaborative teams across the laboratory Ability to function well in a fast-paced research environment, set priorities to accomplish multiple tasks within deadlines, and adapt to ever changing needs Applicants cannot have received their Ph.
D. more than five years prior to the date of application and must complete all degree requirements before starting their appointment. The appointment length will be for up to 24 months with the potential for extension. Initial appointments and extensions are subject to performance and the availability of funding. Please submit three letters of reference when applying to this position. You can upload these directly to your application or have them sent to with the position title and number referenced in the subject line.
Instructions to upload documents to your candidate profile: Login to your account via jobs. ornl. gov View Profile Under the My Documents section, select Add a Document Benefits at ORNL: ORNL offers competitive pay and benefits programs to attract and retain talented people. The laboratory offers many employee benefits, including medical and retirement plans and flexible work hours, to help you and your family live happy and healthy. Employee amenities such as on-site fitness, banking, and cafeteria facilities are also provided for convenience.
Other benefits include: Prescription Drug Plan, Dental Plan, Vision Plan, 401(k) Retirement Plan, Life Insurance, Pet Insurance, Generous Vacation and Holidays, Parental Leave, Legal Insurance with Identity Theft Protection, Employee Assistance Plan, Flexible Spending Accounts, Health Savings Accounts, Wellness Programs, Educational Assistance, Relocation Assistance, and Employee Discounts. If you have difficulty using the online application system or need an accommodation to apply due to a disability, please email: or call 1.866.963. xyz X. This position will remain open for a minimum of 5 days after which it will close when a qualified candidate is identified and/or hired.
We accept Word (. doc,docx), Adobe (unsecured. pdf), Rich Text Format (. rtf), and HTML (. htm,html) up to 5MB in size. Resumes from third party vendors will not be accepted; these resumes will be deleted and the candidates submitted will not be considered for employment. If you have trouble applying for a position, please email is an equal opportunity employer. All qualified applicants, including individuals with disabilities and protected veterans, are encouraged to apply. UT-Battelle is an E-Verify employer.
understanding of recurrent solid tumors in children. The ideal candidate for this opportunity will have experience in animal handling, data collection and data interpretation, along with the availability to work rotating weekends and holidays. You would learn valuable laboratory skills, including: pre-clinical testing, study management, formulation of chemo-therapy treatment, and data analysis.
Job Responsibilities: Performs laboratory experiments as directed using specific and prescribed techniques/protocols. Follows basic protocols, implementing experimental techniques prescribed by supervisor and providing basic troubleshooting where appropriate. Accurately records experimental procedures
and data. May draft results/data for posters, presentations or publications Operates lab equipment. Performs other related duties as assigned in order to meet the goals of the department and institution Maintains regular and predictable attendance Minimum Education and/or Training: Bachelor's degree in relevant scientific area is required Minimum Experience: no experience required St.
Jude Children's Research Hospital has a diverse, global patient population and workforce, built on the principles of diversity, equity and inclusion. Our founder Danny Thomas envisioned a hospital that would treat children of the world-regardless of race, religion or a family's ability to pay. Learn more
about our history and commitment. Today, we continue the mission to advance cures and means of prevention for pediatric catastrophic diseases through research and treatment.
As we accelerate this progress globally, we believe our legacy of diversity, equity and inclusion is foundational to success. With the commitment of leaders at all levels of the organization, we strive to ensure the St. Jude culture, leadership approaches and talent processes are equitable and culturally responsive. View our Diversity, Equity and Inclusion Report to learn about the hospital's roots in diversity, equity and inclusion, where we are today and our aspirations for an even better future.
Other Information St. Jude is an Equal Opportunity Employer No Search Firms St. Jude Children's Research Hospital does not accept unsolicited assistance from search firms for employment opportunities. Please do not call or email. All resumes submitted by search firms to any employee or other representative at St. Jude via email, the internet or in any form and/or method without a valid written search agreement in place and approved by HR will result in no fee being paid in the event the candidate is hired by St. Jude.
Extraordinary support. And a collaborative, bench-to-bedside environment where you can see, firsthand, how your science translates into survival for the children we serve. Quite simply, at St. Jude, we encourage you to dream big and stop at nothing when it comes to finding cures and saving children.
About the Position: During the past five decades, St. Jude has made remarkable progress toward curing childhood cancer and other life-threating diseases. At St. Jude Children's Research Hospital, we know what can be achieved when the brightest scientific minds face the fewest barriers. That's why we provide world-class facilities, st ate-of-the-art technologies, extraordinary support and a
collaborative, bench-to-bedside environment where you can see, firsthand, how our science translates into survival for the children we serve. S t Jude Children's Research Hospital is committed to world-class support for translational research as we seek to identify novel targets for therapeutic intervention and evaluate relevant therapies in a preclinical setting towards improving treatment options for catastrophic diseases of childhood.
We are seeking a Researcher level technologist to join our Preclinical Therapeutics Program (PTP) team , a dynamic group of research technologists focused on providing a com prehensive suite of resource s for preclinical therapeutic development. This
support includes model development and xenograft ing , treatment with novel therapeutics, study observation and therapy response determin ation using imaging readouts and routine data processing.
This is a dynamic laboratory environment where you will work with researchers involved in innovative basic and translational research for the fulfillment of our mission: Finding Cures. Saving Children. What You Bring: A genuine interest in science Some knowledge of basic laboratory procedures A Bachelor's in a science related field A drive to help end pediatric cancer A can do, willing to learn attitude Responsibilities: Perform all assigned tasks in the lab Assist research teams with collection and analysis of data Conduct specific projects to support departmental goals Maintain efficient laboratory operations Collaborate with all stakeholders to ensure laboratory success Develop skills in and perform key procedures relevant to preclinical translational research studies including delivery of therapies, routine surgery, bioluminescence and ultrasound Minimum Education and/or Training: Bachelor's degree in relevant scientific area is required Minimum Experience: State the minimum years of experience required to do this job successfully.
no experience required, but preferred Benefits Your health and well-being are important to us.
That's why St. Jude Children's Research Hospital provides employees with high-quality benefits choices. We are committed to ensuring our benefits are competitive and affordable. St. Jude continues to cover medical premiums for employees and offers low additional costs for dependents. View all the benefits offered including Medical & Prescription Drug Plans, Dental Plan, Vision Plan, Financial Security, Retirement Plan, Living Well - Employee Wellness Program, Time Off Programs, Educational Benefits, Family Friendly Benefits, and Benefits Unique to St.
Jude. Diversity, Equity and Inclusion St. Jude Children's Research Hospital has a diverse, global patient population and workforce, built on the principles of diversity, equity and inclusion. Our founder Danny Thomas envisioned a hospital that would treat children of the world-regardless of race, religion or a family's ability to pay. Learn more about our history and commitment. Today, we continue the mission to advance cures and means of prevention for pediatric catastrophic diseases through research and treatment. As we accelerate this progress globally, we believe our legacy of diversity, equity and inclusion is foundational to success.
With the commitment of leaders at all levels of the organization, we strive to ensure the St. Jude culture, leadership approaches and talent processes are equitable and culturally responsive. View our Diversity, Equity and Inclusion Report to learn about the hospital's roots in diversity, equity and inclusion, where we are today and our aspirations for an even better future. Have More in Memphis Get the best of big-city amenities mixed with all the charm of a small-town feel when you live in Memphis. From our world-renowned music scene to our eclectic mix of food and people.
Memphis is a place our employees are proud to call home. Our region enjoys a cost of living more than 20% lower than the national average and our state places no personal income tax on wages. Plus, Memphians spend five hours less per year in their daily commute compared to the national average. Learn how you can " Have More in Memphis. " Other Information St. Jude is an Equal Opportunity Employer No Search Firms St. Jude Children's Research Hospital does not accept unsolicited assistance from search firms for employment opportunities.
Please do not call or email. All resumes submitted by search firms to any employee or other representative at St. Jude via email, the internet or in any form and/or method without a valid written search agreement in place and approved by HR will result in no fee being paid in the event the candidate is hired by St. Jude.
about the people who use our products. The UX team plays an integral part in gathering insights about the attitudes, emotions, needs, and behaviors of people who use our products to inspire and inform design. We collaborate closely with each other and with engineering and product management to create industry-leading products that deliver value for the people who use them, and for Google's businesses.
As a Quantitative User Experience Researcher (Quant UXR), you'll help inform your team of UXers, product managers, and engineers about user needs. You'll play a critical role in creating useful, usable, and delightful products. You'll work with stakeholders across functions and levels and
have impact at all stages of product development. You will investigate user behavior and user needs using empirical research methods such as logs analysis, survey research, path modeling, and regression analysis.
Quant UXRs vary in background using skills from computer science, quantitative social science, econometrics, data science, survey research, psychology, human-computer interaction, and other fields. You'll combine skills in behavioral research design, statistical methods, and general programming to improve user experience. The Quant UXR community at Google will help you do your best work. You'll have the opportunity to work with and learn from UXRs across Google through regular
meetups, mentor programs, and access to internal research tools. Google Cloud accelerates organizations' ability to digitally transform their business with the best infrastructure, platform, industry solutions and expertise.
We deliver enterprise-grade solutions that leverage Google's cutting-edge technology - all on the cleanest cloud in the industry. Customers in more than 200 countries and territories turn to Google Cloud as their trusted partner to enable growth and solve their most critical business problems. The US base salary range for this full-time position is $139,000-$208,000 bonus equity benefits. Our salary ranges are determined by role, level, and location.
The range displayed on each job posting reflects the minimum and maximum target for new hire salaries for the position across all US locations. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process. Please note that the compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits. Learn more about benefits at Google.
Minimum qualifications: Bachelor's degree in Human-Computer Interaction, Cognitive Science, Statistics, Psychology, Anthropology, related field, or equivalent practical experience. 5 years of experience in an applied research setting, or similar. Experience in programming languages used for data manipulation and computational statistics (Python, R, MATLAB, C , Java, Go), and with SQL. Product research experience in an applied research setting. Preferred qualifications: Master's or Ph D degree in Human-Computer Interaction, Cognitive Science, Statistics, Psychology, Anthropology, or related field.
5 years of experience conducting UX research on products and working with executive leadership (e. g. Director level and above). 3 years of experience managing projects, and working in a large, matrixed organization. Excellent command of research questions within a given domain, and of technical tools for the analysis of data within that field. Proficiency in programming computational and statistical algorithms for large data sets. Demonstrated expertise in descriptive, inferential, and multivariate statistics, including t-test and ANOVA, and experimental design. - Define and measure quantitative UX goals and metrics in collaboration with Designers, Qualitative Researchers, Data Scientists, Engineers and Program Managers.
- Develop code and statistical models to understand user experience. - Conduct empirical research using methods from computer science, quantitative social science, statistics, econometrics, and other fields to understand user behavior and extract meaningful patterns from large data sets. - Examine existing data and product designs to generate hypotheses and plans for high-impact research. - Prioritize and drive research to improve user experience.
Communicate findings to stakeholders in the company. Make research findings convincing and actionable for both research experts and non-experts. Requisition #: 119141581107143366pca3lyuhf
