Hybrid Clinical Project Manager – Project Manager, Clinical Studies

Posted last week

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About the role

  • Independently manage clinical drug trials and medical studies
  • Project planning and execution from A to Z
  • Coordinate the project team across different functional units and countries
  • Serve as the key contact for the client
  • Oversee global vendor management
  • Train and support the project support team

Requirements

  • University degree in a natural science or an equivalent qualification, ideally with a medical focus
  • Professional background in industry (e.g., CRO, pharmaceutical or biotech)
  • 1–3 years of experience in clinical research, monitoring or project management
  • Experience with non-interventional studies (NIS) and academic clinical trials preferred
  • Good knowledge of GCP/ICH, ISO 14155 as well as ISO 20916 and AMG/MDR/IVDR
  • Analytical, solution-oriented and responsible working style
  • Good proficiency in Office applications
  • Strong interpersonal skills and a team player
  • Proactive participation at Alcedis

Benefits

  • Competitive compensation package
  • Permanent employment
  • 30 days of vacation (based on a 5-day workweek)
  • Flexible working hours
  • Overtime compensation
  • Option to work from home up to three days per week (60:40 model)
  • Company bicycle (bike leasing)
  • Capital-forming payments (Vermögenswirksame Leistungen)
  • Additional salary allowance for health promotion
  • Regular company events and team-building activities
  • Learning and development opportunities
  • Monthly #WinAHappening
  • Free electric vehicle charging stations
  • Fruit basket
  • Unlimited beverages

Job title

Clinical Project Manager – Project Manager, Clinical Studies

Job type

Experience level

Junior

Salary

Not specified

Degree requirement

Bachelor's Degree

Location requirements

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