Senior Director, Program Team Lead

Iovance Biotherapeutics

WorldwideFully remoteFull TimeLead, DirectorHealthcare & Telemedicine
USD 270,000–290,000 a yearPosted 2h ago

Why we think you can apply

Hiring model
Open worldwide · the employer states no country restriction
Work from
Anywhere, the UAE included

Posted 2 hours ago · apply link checked 1 hour ago

About the role

Responsibilities

  • Own program strategy and vision from early development through registration and commercialization
  • Frame program decisions around clinical probability of success, regulatory path, and commercial value
  • Chair the cross-functional program team and manage timelines across workstreams
  • Partner with Program Manager to align domain strategy and execution plans across Clinical, Regulatory, Commercial and CMC
  • Own program dashboards and reporting for leadership on status, timelines and open risks
  • Serve as primary strategic voice for assigned programs in governance forums and executive reviews
  • Support due diligence, business development and investor activities for assigned programs

Requirements

  • Advanced degree (PhD, PharmD, MD, MBA or equivalent)
  • 11+ years in clinical drug development with strong oncology CMC experience
  • Experience with CGT products, especially CAR-T, viral and TIL therapies
  • Working knowledge of global clinical and commercial landscape in oncology and cell therapy
  • Track record leading cross-functional teams through development phases and regulatory submissions
  • Proficiency with program and portfolio management tools
  • Ability to influence senior stakeholders without direct authority

Preferred Qualifications

  • Background in program management, strategy or portfolio leadership in biotech
  • Experience with commercial launch planning or lifecycle strategy
  • Engagement with FDA, EMA or other health authorities in oncology or cell/gene therapy

Benefits

  • Annual base salary range of $270,000 to $290,000 USD

About the Company

Iovance Biotherapeutics is the global leader in tumor infiltrating lymphocyte (TIL) cell therapies for solid tumors. It markets Amtagvi, the first FDA-approved one-time treatment for previously treated advanced melanoma.

What we look for

  • Advanced degree (PhD, PharmD, MD, MBA or equivalent)
  • 11+ years in clinical drug development with strong oncology CMC experience
  • Experience with CGT products, especially CAR-T, viral and TIL therapies
  • Working knowledge of global clinical and commercial landscape in oncology and cell therapy
  • Track record leading cross-functional teams through development phases and regulatory submissions
  • Proficiency with program and portfolio management tools
  • Ability to influence senior stakeholders without direct authority
  • Background in program management, strategy or portfolio leadership in biotech
  • Experience with commercial launch planning or lifecycle strategy
  • Engagement with FDA, EMA or other health authorities in oncology or cell/gene therapy
RegulatoryOncologyProgram ManagementClinical ResearchCMCCell Therapy
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