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Senior Director Program Management

ma • Posted 4 days ago
Onsite Full Time Management & Operations

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Associate at Mantell Associates | CGT Specialist Headhunter

Mantell Associates is partnered with an innovative Cell & Gene Therapy organisation, who is seeking an experienced Senior Director of Program Management to lead cross-functional program teams in the development of advanced cell and/or gene therapy programs.

The successful candidate will be responsible for driving strategic planning, execution, and delivery of complex projects across research, CMC, clinical, regulatory, and commercial functions. This is a high-impact role requiring leadership, strategic insight, and deep understanding of the biotech product development lifecycle.

Senior Director of Program Management - Responsibilities:

  • Lead cross-functional program teams including R&D, CMC, regulatory, clinical, commercial, and business development
  • Develop and maintain comprehensive program plans, timelines, budgets, and risk management strategies
  • Act as the primary point of contact for program-level communication and updates to executive leadership and stakeholders
  • Ensure alignment with corporate strategy, milestones, and financial targets
  • Coordinate with CMC, clinical operations, and regulatory affairs to drive IND/CTA submissions, clinical trials, and BLA/MAA readiness
  • Manage external partnerships including CROs, CDMOs, academic collaborators, and licensing partners
  • Drive decision-making through well-prepared governance presentations and scenario planning
  • Anticipate and mitigate program risks and interdependencies
  • Maintain program documentation and ensure compliance with internal governance and regulatory expectations

Senior Director of Program Management - Requirements:

  • Advanced degree in life sciences (PhD, PharmD, MD, or MS); MBA is a plus
  • 10+ years of experience in biotech/pharmaceutical industry, including 5+ years of program management experience
  • Deep expertise in cell and/or gene therapy, including understanding of vector manufacturing, regulatory landscape, and clinical development nuances
  • Experience with rare diseases, oncology, or immunotherapy indications preferred
  • Previous success in global development programs, including FDA and EMA interactions preferred
  • PMP certification or formal project management training preferred
  • Proven track record in leading cross-functional drug development teams from preclinical through clinical and ideally into commercialization
  • Strong leadership, interpersonal, and influencing skills across matrixed organizations
  • Excellent communication, presentation, and organizational skills
  • Experience with tools like MS Project, Smartsheet, or other project planning software

Mantell Associates is a specialist Pharmaceutical and Life Science headhunting firm. For more information on this opportunity, contact us at +44 (0) .

Seniority level

  • Seniority level

    Director

Employment type

  • Employment type

    Full-time

Job function

  • Job function

    Management, Project Management, and Research
  • Industries

    Biotechnology Research, Pharmaceutical Manufacturing, and Medical Equipment Manufacturing

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