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 the 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 trials. Candidates will be expected to demonstrate a commitment to an accelerated career path in Clinical Trial Management.

Key Responsibilities:

• Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager
• Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy
• Compile and maintain project-specific status reports within the clinical trial management system
• Interact with the internal project team, Sponsor, study sites, and third-party vendors
• Provide oversight and quality control of our 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 not required but will be advantageous

Salary (Rate): undetermined

City: London

Country: United Kingdom

Working Arrangements: undetermined

IR35 Status: undetermined

Seniority Level: Entry Level

Industry: Other