Associate Clinical Project Manager

Job Summary

A company is looking for an Associate Clinical Project Manager (DVC).

Key Responsibilities

• Oversee CRO's site management, data management, and monitoring aspects of assigned trials to ensure compliance with regulations
• Assist in writing trial documents, including protocols and informed consent forms
• Review project monitoring status, identify risks, and implement risk mitigation solutions

Required Qualifications

• Bachelor's Degree or equivalent clinical research experience
• Minimum of 5+ years of clinical research experience in academic, industry, or government sectors
• Experience monitoring or providing oversight of clinical trials