Associate Director, Clinical Operations (Fully Remote)

Iovance Biotherapeutics, Inc.

United States

Hybride

USD 150 000 - 230 000

Plein temps

Il y a 3 jours
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Résumé du poste

Iovance Biotherapeutics seeks a senior clinical operations leader to spearhead an integrated team responsible for the execution of oncology-focused clinical programs from conception to final study report.

The role requires strong managerial capabilities, extensive experience with phase 1–4 trials, and the ability to operate in a professional or remote office with up to 20% travel. A fast-paced biotech setting experience is essential.

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.
  • 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.

Responsabilités

  • 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.
  • 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.

Connaissances

Managerial skills
Leadership

Formation

Bachelor's degree in health or science related field

Description du poste

  • 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.
  • 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.

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