Medpace is delighted to host a
Recruitment Event tailored to candidates studying or holding a
PhD in Life Sciences. If you are looking for a transition to the
Clinical Trial Industry, this is a perfect chance for your to explore a career in our Clinical Trial Management team. The Associate Clinical Trial Manager role in Medpace offers the unique opportunity in the research of drug and medical device development to accelerate the development of safe and effective medical therapeutics. Meet Medpace current employees and the management
face-to-face, and discover the potential opportunities we have!
LOCATION: Medpace Singapore Office
DATE: 14 May 2026, Thursday
APPLICATION CLOSE DATE: 28 April 2026, Tuesday
As an aCTM, you will become an integral part of the operational teams for global clinical trials, collaborating with key internal stakeholders - Project Coordinators, Clinical Research Associates, Medical Monitors - and external stakeholders - Sponsors, Clinical Sites and Vendors - to ensure the seamless execution of studies.
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 reserach and development of cutting-edge therapeutics. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).
What to Expect Next:
A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an RSVP.
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 our internal regulatory filing system;
- Provide oversight and management of study supplies;
- Create and maintain project timelines; and
- Coordinate project meetings and produce quality minutes.
Qualifications
- PhD in Life Sciences
- A background in one of our key therapeutic areas if of advantage but not a must:
- Oncology
- Cardiovascular/Renal/Metabolic
- Nuclear Medicine/Radiopharmaceuticals
- Fluency in English with solid presentation skills
- 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
Medpace Overview
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.
Why Medpace
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
