Pharmacokineticist

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives.

Labcorp is seeking a Pharmacokineticist to join our Toxicology team.

Work Schedule: Monday - Friday – 37 hrs

Job Responsibilities:

• Designs and reviews protocol, prepares reports, and carries out kinetic analysis of mostly toxicokinetic/pharmacokinetic studies, occasionally with mentorship and guidance, to develop general expertise in the field
• Conduct kinetic analysis using a noncompartmental approach
• Review analysis plans with clients, including alliance clients and study directors to determine their needs and to suggest/guide plans to accomplish these needs
• Participates in project management responsibilities, including attending client visits, other client interactions, and maintaining strong client relationships, representing the department in technical discussions under the supervision of senior staff
• Provides guidance and leadership to ensure project completion and timely progression
• Reviews technical validity of projects and test results
• Evaluates experimental data and writes scientific reports or oversees report production through finalization, including archival of data
• Assists in the development of departmental policies, procedures, and training manuals
• Trains and mentors pharmacokinetic study coordinators
• Reviews QAU report audits and submits audit responses for SD/management approval
• Ensures that all necessary report/raw data or client comment clarifications are completed
• Maintains positive control over timing and scheduling issues related to every aspect of the study process, including on-time reporting
• Discuss project issues or scope changes with the Study Director, suggest solutions and actions to solve study issues, improve process efficiency, manages the impact on time and cost, reviews protocol changes and communicates the status of changes to client and management, as necessary
• Assures that the final report, including any changes, is approved and in compliance with appropriate SOPs and regulatory agency guidelines
• Provides relevant information to ensure accuracy of forecast and revenue recognition.
• Coordinates small project teams or workstreams to support study execution
• Supports quality control and peer reviews to ensure consistency and compliance
• May begin contributing to departmental planning or capability-building discussions

Minimum Qualifications:

• Degree in Pharmacokinetics, Pharmacodynamics, Biopharmaceutics, Pharmacology, Biomedical Science

Preferred Qualifications:

• Masters in Pharmacokinetics, Pharmacodynamics, Biopharmaceutics, Pharmacology

Additional Job Standards:

• Some level of TK (toxicokinetics) experience, working within a regulated environment
• Some working knowledge of WinNonlin 
• Skilled in writing reports/summarization and data interpretation for regulatory agencies
• Can demonstrate ability for logical thinking, vision, and creativity necessary to function effectively with little structure or supervision
• Has performed scientific presentations and preparing scientific publications
• Effective communication skills
• This is a remote based role

As a Pharmacokineticist you will be responsible for designing and reviewing protocols, conducting and interpreting toxicokinetic/pharmacokinetic analyses (primarily using noncompartmental methods), and preparing high-quality scientific reports in compliance with GLP and regulatory requirements. The position involves managing studies and client relationships, providing technical guidance, ensuring scientific validity and timely completion of projects, and addressing study issues, protocol changes, and reporting requirements. 

Supporting project management activities, quality control and peer review processes, revenue forecasting, and regulatory compliance, contributing to departmental procedures and capability development, and coordinating small project teams to ensure efficient study execution and on-time delivery of results with some guidance from senior staff.

Benefits:

• Competitive salaries
• No weekend work
• Wider benefits package including pension and generous holiday allowance

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:

Labcorp strives for inclusion and belonging 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 and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), 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. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. 

We encourage all to apply

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