Associate Clinical Trial Manager - PhD - Postdoctoral - Nephrology

Medpace; Denver (CO); On-site; USD 60,000 - 100,000; Full time

Job summary

An established industry player is looking for a dedicated Associate Clinical Trial Manager to join their dynamic team in Denver. This full-time, office-based role is perfect for recent PhD graduates in Nephrology or related fields, offering a unique opportunity to apply analytical skills in clinical project management. The company provides extensive training and a clear career path in the exciting field of therapeutics research. Join a passionate organization recognized for its commitment to innovation and employee growth, and make a meaningful impact in the healthcare sector.

Benefits

Flexible work environment

Competitive benefits

Career growth opportunities

Community involvement

Qualifications

• PhD in Life Sciences required.
• Ability to work in a fast-paced, international environment.

Responsibilities

• Communicate and collaborate on global study activities with project teams.
• Ensure timely and accurate completion of tasks.
• Manage study supplies and oversee regulatory filing systems.

Skills

Analytical Skills

Project Management

Communication

Education

PhD in Life Sciences

Job description

Associate Clinical Trial Manager - PhD - Postdoctoral - Nephrology

Job Locations
United States-OH-Cincinnati | United States-TX-Irving (Dallas) | United States-CO-Denver

Category: Clinical Trial Management

Job Summary

Medpace is seeking candidates with Nephrology-related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM). The aCTM will work with the Clinical Trial Management team, Project Coordinators, and Clinical Trial Managers to perform clinical trial activities. Candidates should have a desire to apply their analytical and academic skills in clinical project administration and management.

This role offers a great opportunity for recent PhD graduates to enter the industry, receive foundational training, work internationally, and develop a career in cutting-edge therapeutics research and development. Expect an intensive training period and a potential accelerated career path into Clinical Trial Management.

Responsibilities

1. Communicate and collaborate on global study activities with project teams
2. Ensure timely and accurate completion of tasks
3. Maintain project status reports within the clinical trial management system
4. Interact with internal teams, sponsors, study sites, and vendors
5. Oversee regulatory filing systems
6. Manage study supplies
7. Create and update project timelines
8. Coordinate meetings and produce minutes

Qualifications

• PhD in Life Sciences
• Ability to work in a fast-paced, international environment
• Prior experience in CRO or pharmaceutical industry is advantageous but not required

About Medpace

Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV development services across various therapeutic areas. Headquartered in Cincinnati, Ohio, with over 5,000 employees in more than 40 countries, our mission is to accelerate the development of safe and effective medical therapeutics.

Why Join Medpace?

Join a passionate team committed to making a difference. We offer a flexible work environment, competitive benefits, career growth opportunities, and community involvement. Recognized as a top workplace and a leader in the industry, Medpace values its employees and their contributions.