Related skills
r pharmacokinetics nonmem winnonlin pharmacodynamics๐ Description
- Provide clinical pharmacology expertise to cross-functional teams.
- Conduct non-compartmental PK, pop PK, PK/PD analyses.
- Design and run clinical pharmacology studies (food effect, DDI, AME).
- Co-author regulatory documents (protocols, study reports, IB).
- Collaborate on non-clinical DMPK and translational pharmacology.
- Manage external CROs to ensure adherence to protocols and timelines.
๐ฏ Requirements
- PhD or PharmD with relevant training; 6+ years' experience (Director level).
- Strong PK/PD knowledge and drug metabolism.
- Proficient in WinNonlin, NONMEM, R, and modeling software.
- Experience in preclinical/clinical development of investigational drugs (small molecules/biologics).
- Proven track record in authoring DMPK and Clinical Pharmacology regulatory docs.
- Excellent collaboration, communication, and interpersonal skills.
๐ Benefits
- Paid Time Off, holidays, and sick leave
- Medical, dental, and vision plans
- Short- and long-term disability coverage
- Life/AD&D coverage + voluntary life
- FSA/HSA and commuter benefits
- 401(k) with Erasca match + Employee Stock Purchase Program
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