Temporary Clinical Study Manager

A company is looking for a Temporary Clinical Study Manager.

Key Responsibilities :

Lead and manage the execution of clinical trials, ensuring compliance with regulatory requirements and study deliverables

Develop and manage study timelines, budgets, and vendor relationships while coordinating with cross-functional teams

Oversee clinical monitoring activities and ensure audit-ready documentation throughout the trial lifecycle

Required Qualifications :

Bachelor's Degree in health, biologic science, or a related field

Minimum of 8 years of clinical study management experience in the biopharmaceutical industry, including at least 5 years in a leadership role

Prior experience managing contracted resources and CROs

Experience managing metabolic clinical programs through phases 1-4; oncology experience preferred

Advanced knowledge of GCP and current regulations in the US, EU, and UK