Lead / Manager for Clinical Project Management (m/f/d)

Your strength:

• At least five years of experience as a clinical project manager skilled in organizing, coordinating, and implementing medical device clinical trials
• 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 go to additional efforts to achieve agreed goals

Your contribution:

• Organization, supervision, and execution of clinical project management activities for medical device studies with our products.
• 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 against time, quality, and cost targets

Our strength:

• 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