Clinical Study Manager

Job Summary

A company is looking for a Clinical Study Manager to lead or support post-trial access work within a clinical research team.

Key Responsibilities

• Plan and execute assigned clinical trials in compliance with quality standards, on schedule and within budget
• Oversee strategic partners, CROs, and vendors to ensure adherence to regulatory obligations and business objectives
• Manage study timelines, budgets, and risk mitigation strategies while providing operational input into study documents

Required Qualifications

• Bachelor's Degree or international equivalent required; Life Sciences preferred
• 5+ years of experience in the pharmaceutical industry or clinical research, with at least 3 years in clinical study management
• Experience managing post-trial access and familiarity with global regulatory and compliance requirements
• Demonstrated experience in project/program management, including timeline and budget management
• Experience with early phase clinical studies or Phase 2 and 3 studies is advantageous