Clinical Project Manager overseeing clinical drug trials and studies for major clients. Managing project planning, execution, and team coordination across multiple international sites.
Responsibilities
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)
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