Senior Clinical Trial Manager, Clinical Operations

Iambic Iambic · Pharma · United States · Remote · Clinical

Senior Clinical Trial Manager responsible for operational leadership of early-phase oncology studies, ensuring compliance with global regulatory requirements, ICH-GCP, and company SOPs. This role involves vendor oversight, risk management, timeline and budget performance, and cross-functional alignment within a growth-stage biotech environment.

What you'd actually do

  1. Provide end-to-end operational leadership for complex clinical trials from start-up through close-out, ensuring delivery on time, within budget, and in compliance with global regulations and company SOPs
  2. Lead cross-functional study teams and drive alignment across Clinical Development, Regulatory, Biometrics, and external partners
  3. Develop and execute enrollment, site management, and monitoring strategies to ensure high-quality trial conduct and performance
  4. Oversee CRO and vendor performance, including KPI management, monitoring quality oversight, document review and approval, and vendor selection support
  5. Partner with Data Management and Medical to conduct ongoing data review and ensure timely query resolution

Skills

Required

  • Bachelor’s degree in life sciences or related field
  • 7+ years of progressive clinical trial management experience
  • Experience managing clinical trials from start-up through close-out
  • Experience overseeing global, multi-site studies and CRO partners
  • Oncology clinical trials experience
  • Knowledge of ICH-GCP, FDA/EMA regulations, and global regulatory requirements
  • Proficiency with clinical trial systems (CTMS, eTMF, IRT, EDC, safety databases)

Nice to have

  • solid tumor and early-phase (Phase I/Ib or II) experience

What the JD emphasized

  • oncology clinical trials required
  • ICH-GCP
  • global regulatory requirements