Associate Clinical Trial Manager - PhD / Post-Doc (Cardiovascular/Renal/Metabolic/Gastrointestinal)
Core
Associate Clinical Trial Manager supporting project coordinators and managers in global clinical trial administration and management for biotech/pharma clients.
Role type
Associate Clinical Trial Manager (aCTM)
Builds
Clinical trial management services for biotechnology, pharmaceutical, and medical device industries
Domain
Clinical Research / Contract Research Organization (CRO)
Deliverable
client delivery
Required skills
PhD in Life Sciences, Cardiovascular/Renal/Metabolic/Gastrointestinal research experience, English fluency, project administration, regulatory filing oversight, study supply management, timeline creation, meeting coordination
Preferred skills
Prior CRO or pharmaceutical industry experience
Technologies
Clinical trial management systems, Microsoft Office (Word, Excel, Windows)
Responsibilities
Communicate and collaborate on global study activities; Ensure timely delivery of recurrent tasks; Compile and maintain project-specific status reports; Interact with internal team, Sponsor, study sites, and vendors; Provide oversight of regulatory filing system; Manage study supplies; Create and maintain project timelines; Coordinate project meetings
Seniority
Entry-level / Associate