Associate Clinical Trial Manager (aCTM) Medpace is seeking a candidate with Nephrology related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager to join our France, Lyon Clinical Trial Management team.
Responsibilities Communicate and collaborate on global study activities
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 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
Coordinate project meetings and produce quality minutes
Qualifications PhD in Life Sciences
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
Salary Estimated salary: €60,000 - €80,000 per year
Company Overview Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.
Benefits 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
Why Choose Medpace? Make a difference tomorrow. Develop your career in the research and development of cutting-edge therapeutics.
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