Senior Clinical Pharmacologist (Sr. Scientist)
About The Position
We are seeking a highly motivated Senior Clinical Pharmacologist (Sr. Scientist) to support clinical pharmacology activities with a focus on hands-on technical execution. This is a non-strategic, execution-focused role, ideal for an early-career scientist eager to apply their training in a real-world drug development setting. The successful candidate will work closely with internal leads to deliver PK analyses, data interpretation, and study support, collaborating with cross-functional teams and external partners, including pharmacometrics and CRO groups. You will contribute to the design and interpretation of clinical pharmacology studies, develop a strong understanding of how PK parameters are generated and applied, and help ensure work aligns with regulatory expectations (FDA, EMA, ICH). This position is best suited for someone with a strong foundation in pharmacokinetics and clinical pharmacology who enjoys hands-on analytical work, cross-functional collaboration, and working with external experts.
Requirements
- 1–2 years of relevant industry experience (postdoctoral experience may be considered)
- Experience performing and interpreting noncompartmental pharmacokinetic (NCA) analyses
- Experience authoring PK study reports
- Experience developing, evaluating, and interpreting population pharmacokinetic (PopPK)models, with an understanding of FDAPopPKguidance and regulatory standards
- Experience supporting clinical study execution
- Experience collaborating with cross-functional teams (Clinical Ops, Regulatory, CMC) and/or external partners/CROs
- PhD or PharmD with focus in Pharmacokinetics, Pharmacology, Pharmaceutical Sciences, or a closely related field
- Strong foundation in clinical pharmacology principles, PK, and study design
Nice To Haves
- Experience in antibiotic development
- Proficiency in data analysis and population PK modeling using tools such as R, NONMEM,WinNonlin,orrelated platforms
Responsibilities
- Perform, review, and interpret pharmacokinetic (PK) analyses, including non‑compartmental and model‑informed approaches
- Support the design, execution, and analysis of clinical pharmacology studies in humans
- Contribute to the development, refinement of study protocols,with emphasis on PK-related sections
- Prepare and review clinical pharmacology content for key clinical and regulatory documents, including clinical study reports, regulatory submission modules, and briefing materials (e.g., FDA briefing books)
- Collaborate with cross‑functional teams to address PK‑related questions and support timely delivery of clinical pharmacology outputs
- Interface with external CROs and pharmacometrics partners, managing contracts, reviewing outputs and ensuring quality of deliverables
- Interpret clinical pharmacology data to inform program‑level and dose‑selection decisions
- Apply relevant regulatory guidance to ensure analyses and reporting are compliant, consistent, and scientifically rigorous
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
Ph.D. or professional degree
Number of Employees
11-50 employees
