Associate Clinical Trial Manager - PhD - Cardiovascular - Cincinnati

Medpace is seeking candidates with PhDs and/or Post-Doctoral Researchers with Cardiology experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) position in Cincinnati, OH.

About the role

The aCTM is part of the Clinical Trial Management team, working with Project Coordinators and Clinical Trial Managers to perform clinical trial management activities. This role is ideal for recent PhD graduates looking to transfer and apply analytical and academic skills in clinical project administration and management. It offers solid foundational training, work in an international environment, and career development in the research and development of cutting-edge therapeutics. Candidates should expect an intensive training period and demonstrate 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

Requirements

• PhD in Life Sciences
• Expertise related to cardiomyopathy, lipid disorders, obesity, heart failure, endocrinology, NASH, acute coronary syndrome, CVD, or preventive cardiology
• Ability to work in a fast-paced, dynamic industry within an international team
• Prior experience within the 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 clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through clinical research excellence. We leverage in-country regulatory and therapeutic expertise across major therapeutic areas, including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs over 6,500 people across 40+ countries.

Benefits

• Competitive compensation programs that recognize and reward performance
• Comprehensive health, wellness, retirement, and PTO benefits
• Office-based culture with occasional work-from-home flexibility for eligible positions after training
• Company-sponsored social events and intramural sports
• Defined career paths with clear advancement opportunities
• Industry-renowned onboarding and training programs designed to accelerate professional development
• Ongoing training and continuous learning opportunities throughout your career
• An environment that encourages employees to influence change, contribute ideas, and grow quickly

Cincinnati Headquarters Experience

• A modern corporate campus designed to support collaboration and productivity
• Multiple on-site dining options in the heart of Madison Square
• Free on-site parking
• Convenient access to on-site 24-7 fitness and wellness facilities