What are the responsibilities and job description for the Clinical Trial Manager position at EPM Scientific?
Company Overview
A well‑funded, late‑stage biotech leveraging Nobel Prize-winning science, AI, and automation to transform drug discovery and development. With a lead oncology program advancing into Phase 3 and additional programs in neurology and immunology, the company is scaling its Clinical Operations team to support upcoming pivotal trials. Backed by $1.1B in funding and led by seasoned industry leaders, this is a high‑impact opportunity at a critical growth stage.
Responsibilities
- Lead day‑to‑day operational oversight of global oncology clinical trials in an insourced model
- Partner with cross‑functional teams (Clinical Ops, Medical, Regulatory, Data Science) to drive trial execution
- Oversee study start‑up, site activation, and ongoing site management
- Track timelines, milestones, and trial performance; proactively mitigate risks
- Ensure compliance with ICH‑GCP, regulatory requirements, and internal processes
- Manage vendors (CROs, labs, imaging) as needed
- Support development and maintenance of study documents and trial files
Qualifications
- Experience working as a CTM
- Experience managing oncology clinical trials
- Phase 3 global experience
- Prior experience in an insourced or FSP model
- Fluent in Mandarin or Japanese (strong preference)
If you or someone you know fits this experience and shows interest, we'd love to speak with you!
Salary : $150,000 - $170,000