Summary: The Associate Clinical Trial Manager (aCTM) role at Medpace is designed for candidates with PhDs or Post-Doctoral Research experience, focusing on clinical trial management activities. This full-time, office-based position offers recent graduates an opportunity to apply their analytical skills in a dynamic international environment while receiving comprehensive training. The role involves collaboration with project coordinators and clinical trial managers to ensure the successful execution of clinical studies. Candidates will be expected to manage project timelines, maintain status reports, and oversee regulatory filings.

Key Responsibilities:

• Communicate and collaborate on global study activities with project coordinators and clinical trial managers.
• Ensure timely delivery of recurrent tasks with high accuracy.
• Compile and maintain project-specific status reports within the clinical trial management system.
• Interact with internal project teams, sponsors, study sites, and third-party vendors.
• Manage and perform quality control of the internal regulatory filing system.
• Provide oversight and management of study supplies.
• Create and maintain project timelines.
• Coordinate project meetings and produce quality minutes.

Key Skills:

• PhD in Life Sciences.
• Fluency in English with solid presentation skills.
• Ability to work in a fast-paced dynamic industry within an international team.
• Prior experience within the CRO or pharmaceutical industry is advantageous but not required.

Salary (Rate): undetermined

City: London

Country: United Kingdom

Working Arrangements: undetermined

IR35 Status: undetermined

Seniority Level: Entry Level

Industry: Other