Cardiovascular PhD - Clinical Trial Management Career

Medpace; Warszawa; On-site; PLN 169,923 - 254,885; Full time

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 in Warsaw, Poland. This full-time, office-based role supports clinical trial management activities. Ideal for PhD graduates, you will receive extensive training and the chance to work in an international environment on cutting-edge therapeutics. Responsibilities include coordinating global study activities and maintaining project timelines. Fluency in English is required, and prior experience in the CRO or pharmaceutical industry is advantageous. Medpace offers a flexible work environment with competitive benefits.

Qualifications

• Desire to transfer and apply analytical and academic skills in clinical project administration and management.
• Prior experience within the CRO or pharmaceutical industry is advantageous.

Responsibilities

• Communicate and collaborate on global study activities with project coordinator and clinical trial manager.
• Ensure timely delivery of tasks consistently with accuracy.
• Compile and maintain project-specific status reports within the clinical trial management system.
• Interact with the internal project team, Sponsor, study sites, and third-party vendors.
• Provide oversight and quality control of our internal regulatory filing system.
• Manage study supplies and create project timelines.
• Coordinate project meetings and produce quality minutes.

Skills

Fluency in English

Presentation skills

Ability to work in dynamic industry

Education

PhD in Life Sciences

Job description

Medpace is seeking an Associate Clinical Trial Manager in Warsaw, Poland. This full-time, office-based role supports clinical trial management activities. Ideal for PhD graduates, you will receive extensive training and the chance to work in an international environment on cutting-edge therapeutics. Responsibilities include coordinating global study activities and maintaining project timelines. Fluency in English is required, and prior experience in the CRO or pharmaceutical industry is advantageous. Medpace offers a flexible work environment with competitive benefits.