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

Medpace; Denver (CO); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Medical, dental, vision coverage

401(k) plan

Paid holidays and sick days

Work-from-home flexibility

Pet insurance

Job summary

Medpace is looking for a full-time Associate Clinical Trial Manager (aCTM) position in Denver, CO. The role is an excellent opportunity for recent PhD graduates with a focus on gastrointestinal (GI) conditions. You'll be integral in managing clinical trial activities and collaborating closely with project teams.

Expect intensive training aimed at developing your career in Clinical Trial Management (CTM). The position offers a compensation range of $70,000 - $90,000, alongside various benefits including medical, dental, and work-from-home flexibility.

Qualifications

• PhD in Life Sciences required.
• Experience with gastrointestinal conditions is a plus.
• Ability to work in a fast-paced environment within an international team.

Responsibilities

• Communicate on global study activities with project teams.
• Ensure timely and accurate task delivery.
• Compile and maintain project-specific status reports.

Skills

Analytical skills

Collaboration

Time management

Education

PhD in Life Sciences

Job description

Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Researchers with Gastrointestinal (GI) experience for a full-time office-based Associate Clinical Trial Manager (aCTM) position in Denver, CO.

The aCTM is 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.

This is 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 an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).

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 the internal regulatory filing system
• Provide oversight and management of study supplies
• Create and maintain project timelines
• Coordinate project meetings and produce quality minutes

Qualifications

• PhD in Life Sciences
• Expertise related to gastroparesis, ulcerative colitis, irritable bowel syndrome, Crohn's disease
• 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

Compensation & Benefits

A target salary range of $70,000 - $90,000 with potential for bonus and equity awards. Your compensation will be based on your skills and experience. Medpace offers the following benefits for full‑time positions: medical, dental, vision, 401(k), vacation policy, sick days, paid holidays, work‑from‑home flexibility, short‑term disability, long‑term disability, health savings and flexible savings accounts, life and AD&D insurance, pet insurance, and reimbursement for travel expenses (including food and gas allowance, rental cars, and hotel accommodations).