About the role

  • Project Assistant supporting Clinical Operations in planning and executing clinical trials. Role includes organizing study centers and documentation tasks for clinical research.

Responsibilities

  • Support in organizing the study at investigational sites and supporting investigators
  • Query study status at sites and document findings
  • Train investigators and site documentation staff on the study and the EDC software
  • Conduct feasibility assessments for new projects with study sites
  • Assist in preparing study documents
  • Prepare submissions for regulatory authorities and ethics committees
  • Create and maintain the Study Master File
  • Support sites in handling queries related to electronic study data
  • Correspondence in German and English
  • Ship and track documents and study materials to study sites
  • Draft and revise study contracts
  • Prepare documentation for site compensation/payments
  • Organize investigator meetings
  • Create presentations, charts and tables

Requirements

  • Completed training or education in a medical or commercial/business field
  • Ideally: experience in organizing clinical trials
  • Independent and analytical working style
  • Good knowledge of the MS Office suite
  • Team player with flexibility
  • Excellent communication and organizational skills
  • Good written and spoken English

Benefits

  • 30 vacation days (based on a 5-day workweek)
  • Flexible working hours
  • Overtime compensation / time off in lieu
  • Home office option (up to three days per week)
  • Company bike (bike leasing)
  • Employer contributions to capital-forming payments (VWL)
  • Additional pay for health promotion
  • Regular company events and team-building activities
  • Learning and development options (e.g., Babbel app)
  • Free electric car charging stations
  • Fruit basket
  • Complimentary beverages

Job title

Project Assistant – Clinical Trials

Job type

Experience level

Mid levelSenior

Salary

Not specified

Degree requirement

Professional Certificate

Location requirements

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