Clinical Trial Manager

Iovance Biotherapeutics

WorldwideFully remoteFull TimeMid LevelHealthcare & Telemedicine
USD 145,000–165,000 a yearPosted 4h ago

Why we think you can apply

Hiring model
Open worldwide · the employer states no country restriction
Work from
Anywhere, the UAE included

Posted 4 hours ago · apply link checked 3 hours ago

About the role

Responsibilities

  • Support operational execution of clinical studies from initial synopsis through final deliverables
  • Manage study implementation, timelines, budgets and vendor selection
  • Oversee cross-functional study team members within approved budget and timelines
  • Manage risk and prioritize competing tasks and issues
  • Lead vendor qualification and systems setup including EDC, IWRS and central laboratories
  • Review data for trends and outliers; ensure data integrity through routine reviews
  • Track and communicate program progress to senior management with dashboards and trackers

Requirements

  • Bachelor's degree with 5+ years of pharmaceutical, biotech or clinical research experience
  • At least 1 year as a Clinical Trial Manager
  • Experience designing, initiating and managing phase 1-4 clinical trials
  • Experience managing CROs and vendor selection
  • Strong interpersonal, communication and leadership skills
  • Knowledge of US and global regulations and guidance (ICH-GCP, FDA-CFR)

About the Company

  • Iovance Biotherapeutics develops and delivers tumor infiltrating lymphocyte (TIL) cell therapies for solid tumors, including the FDA-approved Amtagvi.

What we look for

  • Bachelor's degree with 5+ years of pharmaceutical, biotech or clinical research experience
  • At least 1 year as a Clinical Trial Manager
  • Experience designing, initiating and managing phase 1-4 clinical trials
  • Experience managing CROs and vendor selection
  • Strong interpersonal, communication and leadership skills
  • Knowledge of US and global regulations and guidance (ICH-GCP, FDA-CFR)
Risk ManagementProject Managementvendor managementData AnalysisBudgetingClinical TrialsClinical ResearchICH-GCPCRO ManagementFDA Regulations
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