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About the role
Key responsibilities & impact- Lead model-informed drug development strategies supporting therapeutic areas across antibodies, siRNA, and gene therapies
- Inform dose selection, trial design, and regulatory strategy from early development through submission
- Provide significant Pharmacometrics contributions for research and development programs
- Contribute to strategic program development and communicate complex Pharmacometrics strategies and results to development teams
- Design, conduct, or oversee PMx analysis plans
- Apply standardized or advanced scientific techniques to conduct PK, PD, and other quantitative analyses
- Prepare and timely deliver accurate nonclinical or clinical study reports and regulatory submission documents
Requirements
What you’ll need- PhD in Quantitative Pharmacology, Pharmacometrics, Engineering, or a related field with 7+ years of post-doctoral or industry experience; or MS with 9+ years of relevant experience
- Demonstrated expertise in population PK/PD, exposure–response, or mechanistic modeling (systems biology, or QSP) using tools such as NONMEM, Monolix, Simulx, MATLAB/Simbiology and R
- Proven track record of delivering analyses supporting regulatory submissions and engaging directly with agencies (e.g., FDA, EMA, PMDA)
- Hands-on experience with a broad range of quantitative and computational tools
- Strong publication record
- Exceptional communication and interpersonal skills, with the ability to influence and partner effectively across technical and non-technical teams
Benefits
Comp & perks- Annual bonuses or other incentive plans
- Equity awards
- Pension or retirement benefits
- 401(k) company match
- Health and wellness programs
- Fitness centers
- Medical, dental, vision, life and disability insurance benefits
- Paid time off
- Family support benefits
- Reasonable accommodation during the recruitment process where required
