Associate Clinical Trial Manager - PhD - Postdoctoral - Nephrology, Renal - Denver

Medpace, Inc.•Denver, CO

115d•Onsite

About The Position

Medpace is hiring a full-time, office-based Associate Clinical Trial Manager (aCTM) for its Denver, Colorado office. The role is part of the Clinical Trial Management team and works with Project Coordinators and Clinical Trial Managers on clinical trial management activities. It is intended for candidates with Nephrology or Renal-related PhD or postdoctoral research experience who want to apply their analytical and academic skills to clinical project administration and management. The position offers recent PhD graduates foundational training, experience in an international environment, and opportunities to develop a career in research and development of therapeutics. Candidates should expect an intensive training period and demonstrate interest and aptitude for an accelerated path into Clinical Trial Management. The target salary range is $70,000–$90,000, with potential bonus and equity awards; compensation depends on skills and experience.

Requirements

PhD in Life Sciences.
Ability to work in a fast-paced, dynamic industry within an international team.
Desire to transfer and apply analytical and academic skills in clinical project administration and management.
Candidates should demonstrate the desire and aptitude for an accelerated career path into Clinical Trial Management.

Nice To Haves

Nephrology- or Renal-related PhD or postdoctoral research experience.
Prior experience within the CRO or pharmaceutical industry; this is advantageous but not required.

Responsibilities

Communicate and collaborate on global study activities, working closely with the Project Coordinator and Clinical Trial Manager.
Deliver recurring tasks on time and consistently with a high degree of accuracy.
Compile and maintain project-specific status reports in the clinical trial management system.
Interact with the internal project team, Sponsor, study sites, and third-party vendors.
Provide oversight and 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.

Benefits

Medical, dental, and vision coverage.
401(k).
Vacation policy, sick days, and paid holidays.
Work-from-home flexibility; occasional work from home may be available for eligible positions after training.
Short-term and long-term disability.
Health savings and flexible spending accounts.
Life and AD&D insurance.
Pet insurance.
Reimbursement for travel expenses, including food and gas allowance, rental cars, and hotel accommodations.
Competitive compensation programs that recognize and reward performance.
Comprehensive health, wellness, retirement, and PTO benefits.
Company-sponsored social events.
Industry-renowned onboarding and training programs, on-site mentors, ongoing training, and continuous learning opportunities.