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Clinical Study Coordinator (m/w/d)


Clinical Study Coordinator (w/m/d)

Your Tasks:

  • Conduct of clinical trials to ensure compliance with applicable regulations, good clinical practice (GCP) as well as standard operating procedures (SOPs)
  • Support of the Clinical Project Management Team in setup, implementation and conduct as well as continuous oversight of clinical trials
  • Provide administration and maintenance of electronic trial master file (eTMF) and archiving of clinical study documents including eTMF reconciliation
  • Track payments and vendor invoices in collaboration with finance, so we stay on top of study finance
  • Liaise with internal and external parties and study sites and organize study specific meetings and calls


Your Profile:

  • Bachelor’s degree in relevant life science discipline
  • >2 years’ experience in clinical operations and study management within a pharmaceutical company or at a CRO is a must
  • Solid knowledge on the conduct of clinical studies, requirements, regulations and GCP
  • Fluency in written and spoken German and English
  • Excellent organizational skills, well-structured working style
  • Benefits
  • working in our high-performing and international company environment
  • high degree of independence and responsibility for assigned projects
  • You are a team-player and eager to deliver results in a small but effective clinical study team


The gross monthly salary provided for this function is a minimum of € 2.700.- based on full-time employment. Any potential overpayment depends on professional experience and qualifications.


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