As an Associate Clinical Trial Manager at Medpace, you join the Clinical Trial Management team to help oversee global trial activities and ensure timely, accurate execution. You will collaborate with project coordinators, clinical trial managers, sponsors, and sites, applying your analytical and academic background to clinical project administration. This role offers intensive training, international exposure, and a clear path toward advanced CTM responsibilities.
You'll work on coordinating study timelines, quality control, and stakeholder communications to advance cutting-edge therapeutics. This is a hands‐on entry into industry with meaningful impact on patient outcomes.
Flexible work environment
Competitive compensation and benefits package
Competitive PTO packages
Structured career paths with opportunities for professional growth
Company-sponsored employee appreciation events
Employee health and wellness initiatives
Communicate and collaborate on global study activities with project coordinator and clinical trial manager
Ensure timely delivery of recurring tasks with high accuracy
Compile and maintain project-specific status reports in the CTM system
Interact with internal project team, Sponsor, 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
PhD in Life Sciences
Fluency in English with strong presentation skills
Ability to work in a fast‐paced, international team
Prior CRO or pharmaceutical industry experience is advantageous but not required strong communication team collaboration ability to work under pressure clinical trial management regulatory filing processes
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