Clinical Data Manager (m/f/d) - Hechingen, Germany (Hybrid)
Your Strength
- 2-5 years of experience in Clinical Data Management
- Experience in EDC setup, data review, reporting, and database lock
- Ability to manage moderately complex projects or support senior CDMs
- Strong understanding of clinical data management plans and documentation (eCRF, UAT, CCGs, DMP)
- Experience working with CROs, EDC vendors, and other external partners
- Experience with Python and/or R programming is a plus
- Ability to follow processes in line with SOPs and Work Instructions
- Strong organizational and analytical skills
- Fluent in English
- Willingness to work 1-2 days a week from our office in Hechingen, Germany
Your Contribution
- Lead or support CDM activities on assigned studies, from eCRF specification to database lock
- Prepare, moderate, and follow up on Data Review Meetings
- Support quality initiatives and continuous improvement efforts
- Define and maintain study-specific reporting tools and trackers
- Review and approve study-related documents from a CDM perspective
- Ensure high data quality in the EDC system
- Manage data exports for statistical analysis and ensure PDF archiving
- Coordinate with the biostatistician for data validation and reconciliation
- Oversee or perform UAT testing and documentation
- Maintain financial trackers on a study-by-study basis
Our Strength
- A dynamic, international work environment with opportunities for innovation and leadership
- Diverse and challenging projects with significant global impact
- Opportunities for career growth and specialized training programs
- Flexible working conditions, including hybrid working models
- Attractive employee benefits, such as pension plans and EGYM Wellpass
Contact
JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.,
Lotzenäcker 23, 72379 Hechingen
www.artivion.com
