You oversee clinical data management activities with an emphasis on data quality, reporting, and documentation while fostering initiatives for improvement and collaboration with biostatistics.
Anforderungen
- •2-5 years of experience
- •Experience in EDC setup and data review
- •Ability to manage moderately complex projects
- •Strong understanding of clinical data management plans
- •Experience working with CROs and EDC vendors
- •Experience with Python and/or R programming
- •Ability to follow processes in line with SOPs
- •Strong organizational and analytical skills
- •Fluent in English
- •Willingness to work from office in Hechingen
Deine Aufgaben
- •Lead or support CDM activities on studies.
- •Prepare and moderate Data Review Meetings.
- •Support quality initiatives and continuous improvement.
- •Define and maintain reporting tools and trackers.
- •Review and approve study-related documents.
- •Ensure high data quality in the EDC system.
- •Manage data exports for statistical analysis.
- •Coordinate data validation with the biostatistician.
- •Oversee or perform UAT testing and documentation.
- •Maintain financial trackers for each study.
Deine Vorteile
Dynamic international work environment
Diverse challenging projects
Career growth opportunities
Flexible working conditions
Attractive employee benefits
Original Beschreibung
# Clinical Data Manager (m/f/d)
* Hechingen
* Forschung, Entwicklung, Lehre
* Publiziert: 14.05.2025
It's a good feeling to know you're doing your best with purpose every day. At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. Together with surgeons worldwide, we save lives. In doing so, we rely on the strengths of each and every employee. Your strength counts, too: As an important link in the chain, you make a contribution to saving lives together with us. Contribute your strengths and let us grow together.
We are hiring a
**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