At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations.
We are seeking a Bioanalysis Partnership/Alliance Program Manager to join our team. In this position, you will act as the primary interface and liaison between Labcorp Bioanalytical Laboratories globally and the Sponsor's clinical team and bioanalytical group. The role will include direct leadership and representation on behalf of the Sponsor for the regulatory and scientific strategy for bioanalytical execution on the Sponsor's own clinical studies.
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This position is remote and can be located anywhere in the US and UK.
Duties and Responsibilities:
- Responsible for representing the Sponsor as a primary liaison with the Sponsor clinical study teams for all matters relating to bioanalytical planning, execution and reporting
- Provide a clear point of focus and consistency of execution for the Sponsor by informing staff of specific requirements as outlined and agreed to by the Sponsor clinical study teams
- Maintain and monitor all ongoing projects against the Sponsor timetables: the maintenance of Sponsor specific systems and documentation, the maintenance and provision of project tracking tools, and providing status reports and updates in a timely manner to the Sponsor clinical study teams
- Responsible for the final verification of data quality and integrity for the Sponsor clinical study teams
- The primary liaison for harvesting workload forecast information and translating clinical study team plans and timetables into actionable demand forecasts for the Labcorp global bioanalytical organization
- Maintain and develop all aspects of scientific and regulatory knowledge required to provide the rationale for the successful execution of bioanalytical study activities for the Sponsor clinical study teams
- Collaborate with Labcorp Central Laboratory teams to ensure seamless delivery across multiple business units
- Continuous focus and direct involvement with ongoing process excellence programs between Labcorp and the Sponsor
Education and Experience:
- BS in Chemistry or related field
- 5 years industry experience in a relevant field.
- Prior experience in scientific/regulatory oversight for Bioanalytical Clinical sample data generation.
- Demonstrated track record in a regulated environment for GCP and GLP testing
- Proven ability to prioritize and manage time.
- Good communication, collaboration, and influencing skills
- Extensive knowledge of drug development process
Application Window: The application window will close on 5/3/2024.
Pay Range: 120-130K base salary plus annual bonus eligibility.
Benefits: All job offers will be based on a candidate's skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), ESPP, Paid time off (PTO) or Flexible time off (FTO), Commissions, and Company bonus where applicable. For more detailed information, please click here.
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, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
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