Clinical Data Manager

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 an

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!

Brian Russo, [email protected] , T: +41 435 08 39 01

JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.,

Lotzenäcker 23, 72379 Hechingen

www.artivion.com