Clinical Data Manager m/f/d

Your strength:

• A university degree in Life Sciences, Computer Science or related fields
• At least 2 years of experience as Clinical Data Manager (m/f/d) while owning the full responsibility for the DM scope of a clinical study
• Experience with set up, maintenance and lock/freeze of databases for clinical studies
• Extensive experience with the execution of plausibility checks to ensure the quality of the acquired data
• Experience with creating/maintenance of tracking and reporting tools
• Creating relevant CDM documentation (e.g. eCRF specifications, edit/manual checks specifications, data management plan, eCRF completion guidelines, UAT documentation, etc.)
• Experience with programming/execution of R- and/or Python scripts
• Very good knowledge of the relevant national and international regulations, including data protection regulations
• Ability to work independent and structured on multiple projects in parallel
• High motivation and willingness to make additional efforts to achieve the goals
• Enjoy working in teams and with external partners
• Professional knowledge of the English language

Your contribution:

• Responsible for all CDM-related activities accompanying the set-up, execution and close out of clinical studies
• Responsible for the design, validation, maintenance and database lock/freeze of the clinical databases
• Execute UAT, plausibility checks for clinical data, database lock and post-lock activities.
• Responsible for all aspects of clinical data review and reconciliation
• Ensure timely delivery of clinical data for statistical analysis
• Create and maintain regular reporting and tracking tools, as well as reports required on demand
• Create, maintain and file CDM relevant documentation such as eCRF specifications, edit/manual checks specifications, data management plan, eCRF completion guidelines, UAT documentation, etc.
• Represent Clinical Data Management in cross-functional teams including internal and external stakeholders
• Senior CDM: contribute to process development and process improvement initiatives/work groups
• Senior CDM: mentor junior staff within the CDM group

Our strength:

• Exciting and steadily growing product portfolio for vascular therapy
• Varied work in a dynamic team
• Attractive opportunities for advancement
• Freedom for ideas and independent work
• Intensive training in the field of activity

Apply now and join the Artivion team. We are looking forward to you! 

Irmtraud Kögel, jobs.europe@artivion.com, T: 07471 922 349
JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.,
Lotzenäcker 23, 72379 Hechingen
www.artivion.com