high-throughput bioanalysis to meet the discovery needs of our clients. Additional responsibilities include method development and maintaining and optimizing processes to ensure efficiency. Participates in performance of lab-specific assay development, validation and sample analysis Prepares data tables and reports within LIMS Develops and validates LC-MS/MS assays to detect small molecule analytes Provides support in obtaining reference materials, control plasma and project consumables Participates in data transfers, pre-clinical and clinical data management tasks Assists in training personnel in the operation, maintenance, and troubleshooting of equipment Controls appropriate bioanalytical
portion of studies by designing the experimental approach, overseeing the experimental execution, collating, and interpreting scientific data and generating study reports, working in close co-operation with study Sponsors at all stages Carries out laboratory tasks, working with other laboratory staff to progress study-specific experimental work and, as necessary, to support non-study-specific laboratory duties Job Qualifications Bachelor's Degree or higher degree, in a scientific related discipline Minimum of 3 years previous directly related laboratory experience Exceptional analytical and problem-solving capabilities Full understanding of regulatory requirements of study types assigned Excellent written and verbal communication skills in a team environment
analysis. What The Job Entails: Participates in performance of lab-specific assay development, validation and sample analysis Prepares data tables and reports within Laboratory Information Management Systems (Watson™) Provides support in obtaining reference materials, control plasma and project-specific consumables to meet the objectives of the study Participates in data transfers, pre-clinical and clinical data management tasks Assists in training personnel in the operation, maintenance, and troubleshooting of laboratory equipment Contributes to department initiatives, e.
g. process improvements, as required Always complies with the Laboratory Safety Policy Always complies with company
Standard Operating Procedures unless specifically varied in the validation or sample analysis plan May perform study director/PI activities such as: Controls appropriate bioanalytical portion of studies by designing the experimental approach, overseeing the experimental execution, collating and interpreting scientific data and generating study reports, working in close co-operation with study Sponsors at all stages Carries out laboratory tasks, working with other laboratory staff to progress study-specific experimental work and, as necessary, to support non-study-specific laboratory duties Prepares or reviews standard operating procedures for use by the Company, as required Provides scientific
and technical support to colleagues in the Business Development group, as required This may involve participation in client visits, both inbound and outbound Contributes to the training, monitoring and mentoring of staff as necessary Assists with scientific investigations and efforts to troubleshoot/solve assay problems Attends and presents at Scientific Conferences Lead development and validation of Immunoassays, cell-based assays, q PCR, and/or flow cytometry as required, to detect/monitor biologics in clinical and preclinical analysis Highly experienced with performance of PK/PD, ADA and biomarker immunoassays Requirements: Bachelor's Degree or higher degree, in a scientific related discipline Minimum of 5 years relative work experience Exceptional analytical and problem-solving capabilities Full understanding of regulatory requirements of study types assigned Excellent written and verbal communication skills in a team environment
work in either a Patient Service Center or client office. In this role you will provide exceptional customer service, perform skilled specimen collections and be the face of the company. In addition, you will be provided opportunities for continuous growth within the organization.
The schedule for this location is Monday - Friday 7am - 4pm; every other Saturday 8am -12pm Job Duties/Responsibilities: Perform blood collections by venipuncture and capillary techniques for all age groups Collect specimens for drug screens, paternity tests, alcohol tests etc. Perform data entry of patient information in an accurate and timely manner Process billing information and collect payments when required
Prepare all collected specimens for testing and analysis Maintain patient and specimen information logs Provide superior customer service to all patients Administrative and clerical duties as necessary Travel to additional sites when needed Requirements High school diploma or equivalent Phlebotomy certification from an accredited agency is preferred Previous experience as a phlebotomist preferred Proven track record in providing exceptional customer service Strong communication skills; both written and verbal Ability to work independently or in a team environment Comfortable working under minimal supervision Reliable transportation and clean driving record if applicable Flexibility to work overtime
as needed Able to pass a standardized color blindness test If you're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today!
Labcorp is proud to be an Equal Opportunity Employer: As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, interactionual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic.
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soluble protein biomarkers in support of biologic drug development in a GLP environment or similar Highly experienced in flow cytometry including at least 7 color assay development and validation Experienced in cell-based assays including Neutralizing Antibody Assays (Nab) An expert in a GLP environment and all regulatory aspects associated with immunoassays used in biologic drug development Experienced in the use of LIMS/Watson including data downloads for reporting.
Experienced in immunoassay platforms that include three of the following: MSD, ELISA, Luminex, Gyros, Quanterix, Ella Will act as a representative of Pharmaron at scientific conferences and at customer sites Will represent
Pharmaron in professional organizations like AAPS, SOT or ASGCT and may lead subcommittees that publish industry recommendations. Assists in training personnel in the operation, maintenance, and troubleshooting of laboratory equipment Always complies with company Standard Operating Procedures unless specifically varied in the validation or sample analysis plan.
May perform study director/PI activities such as: Controls appropriate bioanalytical portion of studies by designing the experimental approach, overseeing the experimental execution, collating and interpreting scientific data and generating study reports, working in close co-operation with study Sponsors at all stages. Carries
out laboratory tasks, working with other laboratory staff to progress study-specific experimental work and, as necessary, to support non-study-specific laboratory duties.
Prepares or reviews standard operating procedures for use by the Company, as required. Provides scientific and technical support to colleagues in the Business Development group, as required. This may involve participation in client visits, both inbound and outbound. Contributes to the training, monitoring and mentoring of staff as necessary. Assists with scientific investigations and efforts to troubleshoot/solve assay problems. Attends and presents at Scientific Conferences. Lead development and validation of Immunoassays, cell-based assays, and/or flow cytometry as required, to detect/monitor biologics in clinical and preclinical studies associated with drug development.
Education & Experience Ph D + at least 8 years relevant immunoassay experience OR Master of Science in relevant field + at least 11 years relevant immunoassay experience OR Bachelor of Science in relevant field + at least 17 years relevant experience. #LI-RA1
