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Benefits offered by this job
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
Job summary
Medpace is seeking an Associate Clinical Trial Manager (aCTM) in Warsaw, Poland. Candidates should have a PhD in Life Sciences and ideally some experience in the CRO or pharmaceutical industry, but this is not mandatory. The role involves collaboration, management of clinical trial support activities, and an intensive training period is provided. Medpace offers a flexible work environment, competitive compensation, and structured career paths for professional growth.
Qualifications
PhD in Life Sciences is required for this position.
Fluency in English with solid presentation skills is a must.
Candidates should be able to work in a dynamic international team.
Responsibilities
Communicate and collaborate on global study activities.
Ensure timely delivery of tasks with high accuracy.
Maintain project-specific status reports in the system.
Interact with internal project teams and sponsors.
Oversee internal regulatory filing systems.
Manage study supplies effectively.
Create and maintain project timelines.
Coordinate project meetings and produce minutes.
Skills
Analytical skills
Academic skills
Presentation skills
Collaboration
Education
PhD in Life Sciences
Job description
Medpace is seeking an Associate Clinical Trial Manager (aCTM) in Warsaw, Poland. Candidates should have a PhD in Life Sciences and ideally some experience in the CRO or pharmaceutical industry, but this is not mandatory. The role involves collaboration, management of clinical trial support activities, and an intensive training period is provided. Medpace offers a flexible work environment, competitive compensation, and structured career paths for professional growth.