Description

You will lead and manage clinical data management activities for novel targeted oncology therapies, ensuring data accuracy and compliance. You'll collaborate with cross-functional teams, oversee vendors, and drive department initiatives.

Requirements

• MS, BS/BA degree or equivalent in relevant field
• 15+ years direct experience in early-stage or late-stage clinical trials
• Knowledge of clinical databases, standards, medical terminology, and GCP regulations
• Strong leadership, teamwork, and communication skills
• Oncology experience, especially solid tumors, preferred

Responsibilities

• Manage day-to-day CDM activities for clinical trials across phases
• Define project-level data management strategy and ensure data accuracy
• Oversee external vendors and CROs, including scoping and relationship management
• Lead database development, testing, maintenance, and lock/unlock
• Manage and mentor internal data management team members