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)
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