Senior Director Dmpk

in Healthcare + Life Sciences
  • Alameda, CA View on Map
  • Salary: $230,000.00 - $250,000.00
Permanent

Job Detail

  • Experience Level Director
  • Degree Type Doctor of Philosophy (PhD)
  • Employment Full Time
  • Working Type On Site
  • Job Reference 0000014059
  • Salary Type Annually
  • Industry Pharmaceuticals
  • Selling Points

    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.

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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