Clinical Trial Manager
Iovance Biotherapeutics
WorldwideFully remoteFull TimeMid LevelHealthcare & Telemedicine
No salary statedPosted 7 days ago1w agoApply link checked 2 hours ago
Why we think you can apply
- Hiring model
- Open worldwide · the employer states no country restriction
- Work from
- Anywhere, the UAE included
Posted 7 days ago · apply link checked 2 hours ago
About the role
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.
What we look for
- Bachelor's degree
- 5+ years pharmaceutical or biotech clinical research experience
- 1+ year as CTM
- Experience managing Phase 1-4 clinical trials
- CRO and vendor selection experience
- Knowledge of ICH-GCP, FDA-CFR, and Global Regulations
Clinical TrialsOncologyICH-GCPFDA CFRCRO Management
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Iovance Biotherapeutics
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