Associate Clinical Trial Manager – at Medpace, Apply Now!
Join Medpace, a global leader in clinical research, as an Associate Clinical Trial Manager (aCTM) in Singapore. This role is ideal for PhD holders in nuclear medicine, radiopharmaceuticals, or radiation oncology who want to drive cutting-edge clinical research in radiopharmaceuticals. If you have strong project management skills and an interest in clinical trial administration, apply today to contribute to life-changing therapeutics in the pharmaceutical industry.
About The Company
Medpace is a full-service clinical contract research organization (CRO) that provides Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, with a global presence across 40+ countries and employing over 5,000 professionals, Medpace accelerates the global development of safe and effective medical therapeutics. The company focuses on various therapeutic areas including oncology, cardiology, metabolic diseases, CNS disorders, anti-viral, and anti-infective treatments.
- Job Posting: Associate Clinical Trial Manager (PhD, nuclear medicine / radiopharmaceuticals / radiation oncology)
- Location: Singapore
- Category: Clinical Trial Management
- Job ID: 10821
Job Summary
Medpace is seeking candidates with PhDs or Post-Doctoral Research experience in nuclear medicine, radiopharmaceuticals, or radiation oncology to join as a full-time Associate Clinical Trial Manager (aCTM) in Singapore. The role involves collaborating with the Clinical Trial Management team, engaging in clinical project administration, and contributing to the research and development of cutting-edge radiopharmaceuticals.
Responsibilities
- Communicate and collaborate on global study activities
- Ensure timely delivery of tasks with accuracy
- Maintain project-specific status reports
- Interact with project team, sponsors, study sites, and vendors
- Provide oversight on regulatory filing systems and study supplies
- Create and manage project timelines
- Coordinate project meetings and document minutes
Qualifications
- PhD in Life Sciences (nuclear medicine/ radiopharmaceuticals/ radiation oncology or related)
- Fluency in English with strong presentation skills
- Ability to work in a fast-paced international industry
- Previous CRO or pharmaceutical industry experience advantageous
Medpace Overview
Medpace is dedicated to advancing medical therapeutics globally through its scientific and disciplined approach across major therapeutic areas. With a focus on patient impact, Medpace offers a dynamic working environment that encourages professional growth and development.
Why Medpace?
Medpace values people, purpose, and passion in making a difference in the future of healthcare. Join a team that has positively impacted the lives of countless patients and offers a range of employee perks and benefits.
Medpace Perks
- Flexible work environment
- Competitive compensation and benefits
- Structured career paths and growth opportunities
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
Keywords: Associate Clinical Trial Manager, Medpace Careers, Radiopharmaceutical Research, Nuclear Medicine, Clinical Research, Oncology Trials, CRO Jobs Singapore, Clinical Trial Management, Life Sciences, PhD Jobs in Singapore.
