Lead impactful DMPK initiatives driving pharmaceutical innovation and regulatory success. Collaborate with multidisciplinary teams to optimize drug development strategies. Foster scientific excellence and mentorship within a dynamic organization.
Senior Director Dmpk
in Healthcare + Life Sciences PermanentJob Detail
Job Description
Overview
- Lead the strategic direction of DMPK to enhance drug development processes and regulatory success.
- Drive innovation in pharmacokinetics and pharmacodynamics to optimize therapeutic candidates.
- Collaborate with cross-functional teams to integrate DMPK insights into project strategies.
- Provide mentorship to develop expertise and foster growth within the DMPK team.
- Engage with the scientific community through publications and presentations to maintain visibility.
- Stay updated on advancements in DMPK research to apply cutting-edge methodologies.
- Promote a collaborative and innovative culture within the organization.
Key Responsibilities & Duties
- Lead ADME studies to support IND and NDA submissions, ensuring data accuracy and compliance.
- Analyze pharmacokinetic and pharmacodynamic data to inform drug development strategies.
- Collaborate with discovery teams to refine translational approaches for candidate molecules.
- Partner with clinical pharmacology to ensure seamless transitions into development phases.
- Prepare high-quality regulatory documents, including IND, CTA, and NDA filings.
- Conduct due diligence evaluations through scientific assessments and reviews.
- Deliver impactful presentations to stakeholders, showcasing DMPK contributions.
- Ensure adherence to safety policies and promote best practices in laboratory environments.
Job Requirements
- PhD in Pharmacokinetics, Drug Metabolism, or Pharmaceutical Sciences required.
- Minimum 12 years of DMPK experience, with 14 years preferred in the pharmaceutical industry.
- Expertise in in vitro and in vivo ADME studies, including modeling and simulations.
- Proven experience managing external DMPK work at CROs effectively.
- Extensive experience with regulatory submissions including IND, NDA, and BLA.
- Strong leadership skills with a track record of team management and decision-making.
- Excellent communication skills to foster collaboration across multidisciplinary teams.
- Commitment to staying updated with industry trends and advancements in DMPK research.
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