Associate Clinical Trial Manager (PhD/Postdoctoral) - Cardiovascular, Renal, GI

Medpace; Irving (TX); On-site; USD 60,000 - 100,000; Full time

Job summary

An innovative clinical research organization is seeking a dedicated Associate Clinical Trial Manager to join their dynamic team. This role is perfect for recent PhD graduates eager to transition into the industry, offering extensive training and international opportunities. You will collaborate with talented professionals to manage clinical trial activities, ensuring timely and accurate project execution. With a focus on cutting-edge therapeutics, this position provides a pathway to impactful career growth in a supportive and flexible work environment. Join a passionate team committed to making a difference in healthcare!

Benefits

Flexible work environment

Competitive PTO (20+ days)

Comprehensive benefits

Employee events

Wellness initiatives

Community involvement

Career growth opportunities

Qualifications

• PhD or Post-Doctoral Research experience in Cardiovascular, Renal, or GI areas.
• Ability to work in a fast-paced, international environment.

Responsibilities

• Coordinate global study activities with project teams.
• Ensure timely, accurate completion of tasks.
• Maintain project status reports in the clinical trial system.

Skills

Analytical Skills

Project Management

Communication Skills

Education

PhD in Life Sciences

Job description

Associate Clinical Trial Manager (PhD/Postdoctoral) - Cardiovascular, Renal, GI

Medpace is seeking candidates with PhDs and/or Post-Doctoral Research experience in Cardiovascular, Renal, or Gastrointestinal areas for a full-time, office-based Associate Clinical Trial Manager (aCTM). The aCTM collaborates with Project Coordinators and Clinical Trial Managers to perform clinical trial activities. Candidates should have a desire to apply analytical and academic skills in clinical project management.

This role offers recent PhD graduates a chance to enter the industry, receive foundational training, work internationally, and develop careers in cutting-edge therapeutics R&D. Expect intensive training and an accelerated pathway into Clinical Trial Management.

Responsibilities

• Coordinate global study activities with project teams
• Ensure timely, accurate completion of tasks
• Maintain project status reports in the clinical trial system
• Interact with internal teams, sponsors, sites, and vendors
• Oversee regulatory filings and study supplies
• Create and manage project timelines
• Organize meetings and document minutes

Qualifications

• PhD in Life Sciences
• Expertise in cardiomyopathy, lipid disorders, obesity, heart failure, endocrinology, NASH, acute coronary syndrome, CVD, or preventive cardiology
• Ability to work in a fast-paced, international environment
• Experience in CRO or pharma industry is advantageous but not required

About Medpace

Medpace is a full-service CRO providing clinical development services from Phase I-IV for biotech, pharma, and medical device industries. Headquartered in Cincinnati, Ohio, with over 5,000 employees across 40+ countries, we focus on accelerating the development of safe and effective therapeutics using a scientific, disciplined approach.

Why Join Us?

Join a passionate team making a difference. Benefits include flexible work environment, competitive PTO (20+ days), comprehensive benefits, employee events, wellness initiatives, community involvement, discounts, and career growth opportunities. Recognized as a Top Workplace and by Forbes as a leading midsize company, we value our employees and their contributions.

Next steps involve a review of your qualifications and potential contact for further discussion. EO/AA Employer M/F/Disability/Vets.