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

Your strength:

At least five years of experience as a clinical trial manager skilled in organizing, coordinating, and implementing medical device PMCF studies and clinical investigations
Experience in personnel management including setting goals, monitoring progress, motivating and talent development
Strong knowledge of national and international standards and regulations governing clinical trials
Experience in negotiating clinical study contracts in Europe and Asia-Pacific
Experience in communicating with internal cross-functional teams and external business partners including clinicians and research coordinators
High energy, proven sense of urgency, self-motivation, and willingness to make additional efforts to achieve agreed goals

Your contribution:

Organization, supervision, and execution of clinical trialmanagement activities for medical device trials in the endovascular and cardiac space
Ensuring compliance with internal standards and international regulatory requirements for planned medical device studies in Europe and Asia-Pacific
Ensuring a high quality of conducted studies and readiness for regulatory audits
Supervision of contract negotiations and regulatory approvals of clinical studies
Developing clinical trial timelines and budgets including monitoring performance vs. plan on a quarterly basis
Lead planning and communication with cross-functional teams
Present updates on study progress and clinical results to management
Ensuring study teams deliver on time, quality, and cost targets

Our strength:

An exciting field of activity in a challenging clinical environment
An autonomous area of responsibility
Active participation in an international clinical team
Intensive training with mentoring program
Diverse benefits such as mobile working, job bike and company pension

Apply now and join the Artivion team. We look forward to hearing from you!

Apply now!
Ina Müller, jobs.europe@artivion.com , T +49 (0)7471 922 441
JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.
Lotzenäcker 23, 72379 Hechingen, www.artivion.com