Associate Clinical Trial Manager - PhD - Gastrointestinal (GI) - Denver

Medpace, Inc.•Denver, CO

115d•Onsite

About The Position

Medpace is seeking candidates with a PhD and/or postdoctoral research experience in gastrointestinal (GI) areas for a full-time, office-based Associate Clinical Trial Manager position in Denver, Colorado. The Associate Clinical Trial Manager is part of the Clinical Trial Management team and works with Project Coordinators and Clinical Trial Managers on clinical trial management activities. The role is suited to candidates who want to apply their analytical and academic skills to clinical project administration and management. The position offers recent PhD graduates foundational training, work in an international environment, and the opportunity to develop a career in research and development of therapeutics. Candidates should expect an intensive training period and demonstrate the desire and aptitude to pursue an accelerated career path into Clinical Trial Management. Medpace is a full-service clinical contract research organization providing Phase I–IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. The company says it employs more than 6,500 people across more than 40 countries.

Requirements

PhD in Life Sciences.
Expertise related to gastroparesis, ulcerative colitis, irritable bowel syndrome, or Crohn’s disease.
Ability to work in a fast-paced, dynamic industry within an international team.

Nice To Haves

Prior experience within a CRO or pharmaceutical industry is advantageous but not required.
Postdoctoral research experience in gastrointestinal areas.

Responsibilities

Communicate and collaborate on global study activities, working closely with the project coordinator and clinical trial manager.
Ensure recurrent tasks are delivered 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 meeting minutes.

Benefits

Target salary range of $70,000–$90,000, with potential for bonus and equity awards; compensation is based on skills and experience.
Medical, dental, and vision coverage.
401(k).
Vacation policy, sick days, and paid holidays.
Work-from-home flexibility; the broader benefits description notes occasional work from home 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.
Company-sponsored social events.
On-site mentors, defined career paths, onboarding and training programs, and ongoing learning opportunities.