Associate Clinical Trial Manager (PhD/Post‑Doc) – Cardiovascular, Renal, Metabolic, GI

About the role

Medpace is seeking a recent PhD graduate or post‑doctoral researcher to join its Clinical Trial Management team in Taipei as an Associate Clinical Trial Manager (aCTM). The role offers intensive training and a fast‑track career path in clinical project administration, supporting global studies in cardiovascular, renal, metabolic and gastrointestinal therapeutics.

Key responsibilities

• Collaborate with Project Coordinators and Clinical Trial Managers on global study activities.
• Ensure timely delivery of recurring tasks with high accuracy.
• Compile and maintain project status reports in the clinical trial management system.
• Interact with internal teams, sponsors, study sites and third‑party vendors.
• Oversee quality control of internal regulatory filing systems and manage study supplies.
• Create and maintain project timelines, coordinate meetings and produce detailed minutes.

Required profile

• PhD in Life Sciences with research experience in cardiovascular, renal, metabolic or gastrointestinal areas.
• Fluent English with strong presentation abilities.
• Ability to thrive in a fast‑paced, international environment.
• Prior CRO or pharmaceutical experience is a plus but not mandatory.

Required skills

• Excel
• Word processing
• Databases
• Windows operating system

What we offer

• Comprehensive on‑the‑job training and mentorship.
• Opportunity to work in an international, multidisciplinary team.
• Exposure to cutting‑edge therapeutic development across multiple disease areas.