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Overview:
- Lead the assigned clinical operations team and play a key role in departmental strategy.
- Ensure timely execution of clinical research programs from conception through final study report.
Key Responsibilities:
- Oversee clinical trial agreements, budgets, expenditures, and payments for clinical studies.
- Supervise external contract organizations for site interaction, monitoring, data management, and other critical activities.
- Maintain oversight of study conduct at centers, including site selection, start-up, and closure.
Qualifications:
- Bachelor's degree in health or science related area; 8+ years of pharma/biotech or clinical research experience.
- Demonstrated managerial skills and experience leading phase 1-4 trials, with oncology experience required.
Work Environment:
- Operates in a professional or remote office environment with up to 20% travel.
- Requires standard office equipment and keyboard use, with ability to work in a fast-paced biotechnology setting.
Iovance Biotherapeutics
Iovance Biotherapeutics is the global leader in innovating, developing, and delivering tumor infiltrating lymphocyte (TIL) cell therapies for patients with solid tumors. As an end-to-end cell therapy company with fully owned, centralized U.S.-based manufacturing, it operates with a fast-paced, collaborative culture focused on bringing first-in-class treatments to cancer patients.