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Senior Director, Program Management, CMC

Posted 2024-11-16

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💎 Seniority level: Senior, At least 10+ years of pharmaceutical industry experience

🔍 Industry: Pharmaceutical

🏢 Company: Centessa Pharmaceuticals, LLC

🗣️ Languages: English

⏳ Experience: At least 10+ years of pharmaceutical industry experience

Requirements:
  • 10+ years of pharmaceutical industry experience, preferably in small molecule development.
  • 5+ years of project management leadership experience focused on CMC-related activities.
  • Strong understanding of drug development processes and cGMP requirements.
  • Organizational and analytical skills to manage multiple projects independently.
  • Decision-making and communication skills to coordinate CDMO activities effectively.
  • Excellent oral and written communication skills for scientific information.
  • Project management professional (PMP) certification preferred.
  • Expertise in MS Office including Excel, PowerPoint, and MS Project.
Responsibilities:
  • Serve as main contact for CMC project communications with internal teams and CDMOs.
  • Participate in teleconferences to maintain relationships and track progress.
  • Monitor timelines and contracts, address discrepancies.
  • Support CMC activities, track GMP and Regulatory documentation.
  • Interface with various departments to ensure timely project delivery.
  • Identify resource constraints and risks impacting timelines.
  • Coordinate shipment/logistics and manage detailed project plans.
  • Oversee project objectives and milestones while managing changes.
  • Facilitate collaboration across functional teams.
  • Communicate project updates to stakeholders.
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