Temporary Clinical Study Manager

Job Summary

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