Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time Associate Clinical Trial Manager (aCTM -Cardiovascular, Renal & Metabolic Disease (CVRM)) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management. A fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).

• 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

• PhD in Life Sciences- • Fluency in English with solid presentation skills • Experience in Cardiovascular, Renal & Metabolic Disease studies required; • 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

For more details, please refer to the company website.