The Clinical Trial Manager (CTM) position performs as project lead for multiservice clinical trials (some global in scope).  The position interacts with sponsors and manages the timeline and all project deliverables.  This role coordinates all services contracted for the study.  CTMs are also responsible for leading a team of CRAs and managing project coordinators.

• Direct all operations of designated functional area, department, geographic region, or group of employees; 
• Contribute to overall success and profitability of organization;
• Review analyses of activities, costs, operations, and forecast data to determine progress toward stated goals and objectives; 
• Coordinate functions and activities between departments to ensure contracts/projects awarded to Medpace are successfully completed; 
• Conduct policy training and ensure employees are working in compliance with SOPs, Good Clinical Practice (GCP) and/or Good Laboratory Practice (GLP);   
• Recognize major departmental successes and failures and resolve accordingly; 
• Ensure the organization and its services are consistently presented in strong, positive image to relevant stakeholders and the general public;   
• Evaluate departmental capacity needs on an ongoing basis and coordinate/delegate workload efficiently and in accordance with given timelines; 
• Represent department/functional area in Business Development. Includes review of proposals and participation in general capabilities meeting and BID defense meetings; and 
• Maintain Medpace departmental SOPs to ensure they are present and appropriate.  

• Bachelor’s degree in a health related field (Master’s degree or PhD is preferred);

• Minimum 2 years of clinical trial management experience in Asia Pacific region ideally in a CRO environment;

• Demonstrated ability to think strategically;

• Demonstrated ability to conceptualize and execute organizational strategy;
• Advanced knowledge of federal regulations regarding clinical studies and the conduct of such studies;
• Advanced knowledge of relevant Medpace SOPs, GCP and/or GLP guidelines. 

Medpace is a full-service clinical contract research organization (CRO). We provide 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

• Flexible work environment 
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

Awards

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.