Associate Clinical Trial Manager - PhD/Post-Doc (Cardiovascular/Renal/Metabolic/Gastrointestinal)
Core
Associate Clinical Trial Manager supporting project coordinators and clinical trial managers in global study activities, regulatory filings, and study supply management for biotech/pharmaceutical clinical trials.
Role type
Associate Clinical Trial Manager (aCTM)
Builds
Clinical trial management services for biotechnology and pharmaceutical companies
Domain
Clinical Research / Contract Research Organization (CRO)
Deliverable
client delivery
Required skills
PhD in Life Sciences, Research experience in Cardiovascular/Renal/Metabolic/Gastrointestinal areas, Project administration, Regulatory filing oversight, Study supply management, Timeline creation, Meeting coordination
Preferred skills
Prior CRO or pharmaceutical industry experience, Fluency in English with presentation skills
Technologies
Clinical trial management systems
Responsibilities
Communicate and collaborate on global study activities, Ensure timely delivery of recurrent tasks, Compile and maintain project-specific status reports, Interact with internal project team, Sponsor, study sites, and third-party vendors, Provide oversight and quality control of internal regulatory filing system, Provide oversight and management of study supplies, Create and maintain project timelines, Coordinate project meetings and produce quality minutes
Seniority
Entry-level / Associate
