
Senior Director, Program Team Lead
Iovance Biotherapeutics
WorldwideFully remoteFull TimeLead, DirectorHealthcare & Telemedicine
USD 270,000–290,000 a yearPosted 2 hours ago2h agoApply link checked 1 hour 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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Iovance Biotherapeutics
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