Lead / Manager for Clinical Project Management

Ihre Aufgaben

• 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

Ihr Profil

• 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

Kontakt

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