Clinical Project Manager
Core
Planning, implementation, and management of multiple clinical studies in oncology, overseeing day-to-day operations and managing external Clinical Research Organizations (CROs).
Role type
Senior Clinical Project Manager
Builds
Clinical trials for oncology, urology, women's health, rare diseases, cell & gene therapies, and CNS
Domain
Pharmaceutical / Clinical Research / Oncology
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical trial management, CRO oversight, regulatory compliance (GCP), budget management, cross-functional leadership, protocol review, site selection, change order evaluation, risk mitigation, stakeholder communication
Preferred skills
BS or MS in life science, oncology therapeutic area expertise, matrix environment experience, mentoring
Technologies
Clinical trial management systems, regulatory submission tools, project management software
Responsibilities
Design and deliver clinical studies to agreed timelines; oversee CROs, consultants, and vendors; monitor clinical data collection and study progress; prepare and review study documents (protocols, CSRs, regulatory submissions); manage study budgets and contracts; coordinate clinical trial supplies; evaluate CRO/vendor performance; provide input during regulatory inspections.
Seniority
Senior, hands-on IC with leadership responsibilities