Clinical Trial Manager

Iovance Biotherapeutics

Completely RemoteFull TimeHealthcare & Telemedicine
Posted Today

Job description

Responsibilities

  • Support operational execution of clinical studies from synopsis through final project deliverables
  • Manage implementation, budget, milestones, and timelines for clinical studies
  • Oversee cross-functional study teams to ensure execution within budget and timelines
  • Lead vendor identification, qualification, and selection for EDC, IWRS, and Central Laboratories
  • Ensure data integrity through routine reviews, query resolution, and consistency checks
  • Track and communicate program progress to Senior Management via dashboards and trackers
  • Assess the impact of changing regulations and guidance on clinical projects

Requirements

  • Bachelor's degree
  • 5+ years of pharmaceutical or biotech-related clinical research or oncology experience
  • At least 1 year of experience as a Clinical Trial Manager (CTM)
  • Demonstrated experience designing and managing Phase 1-4 clinical trials
  • Experience in the management and selection of CROs and vendors
  • Subject matter expertise in US and Global Regulations (SOPs, ICH-GCP, FDA-CFR)

About the Company

Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer.

Skills & tools

Clinical TrialsOncologyICH-GCPFDA CFRCRO Management

What the team is looking for

Use this list as a quick fit check before you apply.

  1. 01Bachelor's degree
  2. 025+ years pharmaceutical or biotech clinical research experience
  3. 031+ year as CTM
  4. 04Experience managing Phase 1-4 clinical trials
  5. 05CRO and vendor selection experience
  6. 06Knowledge of ICH-GCP, FDA-CFR, and Global Regulations
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