What are the responsibilities and job description for the Clinical Pharmacology and Pharmacometrics Director position at EPM Scientific - Phaidon International?
A leading biotechnology firm focuses on developing innovative cancer therapies that target specific molecular pathways to improve patient outcomes. Their approach combines cutting-edge research with a deep understanding of cancer biology, advancing treatments that address significant unmet medical needs. With a diverse pipeline of both small molecules and biologics, the company strives to bring forward therapies that can make a meaningful impact on patients' lives. Through collaboration and scientific excellence, they are at the forefront of transforming cancer care with novel, precision-based treatments.
Key Responsibilities
- Develop and execute clinical pharmacology and pharmacometrics strategies to advance Exelixis programs through all stages, from research to post-marketing.
- Serve as the clinical pharmacology lead on project teams, offering expertise in pharmacokinetics (PK) / pharmacodynamics (PD), biopharmaceutics, drug-drug interactions, and quantitative pharmacology.
- Guide the progression of small molecules and biologics through key development milestones, including IND / CTA submissions, EOP2 meetings, and marketing applications.
- Lead or oversee PK / PD and exposure-response analyses using advanced modeling and simulation techniques to support human PK predictions, dose selection and optimization, trial designs, risk / benefit assessments, Go / No-Go decisions, regulatory submissions, and publications.
- Collaborate with cross-functional teams, including Clinical Development, Biostatistics, Discovery, Translational Medicine, CMC, Toxicology, DMPK, Clinical Operations, and Regulatory Affairs, to meet project and corporate objectives.
- Drive the visibility of Exelixis' scientific expertise through publications and external collaborations.
- Work with both internal and external scientific experts to evaluate and implement new methodologies, maintaining cutting-edge techniques, models, and capabilities.
- Ensure adherence to SHE policies, GxP compliance, and regulatory standards throughout the clinical pharmacology programs.
Experience
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