PhD & Postdoctoral Virtual Career Event: Associate Clinical Trial Manager - Cardiovascular, Renal, Gastrointestinal - January 29

Medpace•Cincinnati, OH

3d•Onsite

About The Position

Medpace is delighted to host a Virtual Recruitment Event tailored to candidates studying or holding a PhD in Life Science areas, working within Cardiovascular, Nephrology / Renal or Gastrointestinal (GI) research areas. This is an exciting opportunity for individuals seeking to make a switch from academia to the Clinical Trials Industry ! LOCATION: Virtual - Microsoft Teams Link will be shared with candidates selected to attend. DATE: January 29, 2026 at 5:30 pm eastern time. Please include your resume and attach a cover letter with your application. Associate Clinical Trial Manager At this event, Medpace is seeking to meet candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) role to join our global Clinical Operations team. The aCTM will be working closely 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. This is a fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and accelerate 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). What to Expect Next: A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an RSVP.

Requirements

PhD in Life Sciences area is required; upcoming PhD graduates or Postdocs are welcome to apply!
A background in one of our key therapeutic focus areas: Cardiovascular, Renal / Nephrology, GI/Gastrointestinal/Gastroenterology
Fluency in English with solid presentation skills
Ability to work in a fast-paced dynamic industry

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