Clinical Research Associate III (m/f/d)

JOTEC GmbH 2016; Stein; Hybrid; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A global medical device company located in Germany is seeking a Clinical Research Associate III with a focus on monitoring clinical trials. The ideal candidate should have at least 4 years of experience and the ability to manage multiple study sites independently. This role requires fluency in both German and English, as well as strong communication and organizational skills. Candidates can expect attractive benefits and career growth opportunities in a supportive environment.

Leistungen

Pension plan

EGYM Wellpass

Flexible working conditions

Career growth opportunities

Qualifikationen

• Minimum of 4 years of experience in clinical research monitoring.
• Ability to manage multiple study sites independently.
• Strong organizational skills and ability to manage multiple priorities.

Aufgaben

• Independently manage all phases of site activities.
• Conduct monitoring visits and ensure compliance at investigational sites.
• Build strong relationships with investigators and site personnel.
• Mentor junior CRAs and contribute to process improvement.

Kenntnisse

Clinical research monitoring

Knowledge of regulations (ISO 14155, GCP, MDR, EU, FDA)

Site management

Communication skills

Collaboration and mentorship

Organizational skills

Fluency in German

Fluency in English

Jobbeschreibung

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 aClinical Research Associate III (m/f/d) – Location: EMEA (Flexible).

Your Strength

• Minimum of 4 years of advanced experience in clinical research monitoring
• In-depth knowledge of regulations and guidelines related to clinical trials on human subjects (e.g., ISO 14155, GCP, MDR, EU, FDA)
• Ability to manage 10–15 study sites independently, from start-up to closure
• Excellent communication skills for site interaction, training, and issue resolution
• Strong collaboration and mentorship abilities — CRA IIIs are expected to guide junior team members
• Hands‑on experience with monitoring systems, data verification, and compliance tracking
• Strong organizational skills and the ability to manage multiple priorities
• Willingness to travel for site visits and meetings
• Fluency in German and English is required. Proficiency in the language of one of Germany’s neighboring countries is an advantage, to support potential cross-border monitoring activities.

Your Contribution

• Independently manage all phases of site activities: identification, start‑up, monitoring, and close‑out
• Conduct monitoring visits in line with study plans and regulatory requirements
• Ensure compliance at investigational sites and act as the primary contact for site staff
• Build and maintain strong relationships with investigators and site personnel
• Identify risks, provide solutions, and ensure timely resolution of study‑related issues
• Perform data review and verification for patient safety and protocol adherence
• Conduct site training, initiate visits, and support audit/inspection readiness
• Collaborate with other departments such as Data Management, Clinical Operations, and Medical Affairs
• Support investigator and coordinator meetings, and provide training or presentations as needed
• Mentor junior CRAs and contribute to continuous process improvement
• Participate in CAPA execution, audits, and ongoing quality assurance activities

Our Strength

• A purpose-driven Clinical Affairs team committed to quality and patient safety
• Onboarding and development in a structured, supportive environment
• Exposure to international clinical trials and cross-functional collaboration
• Flexible working conditions and career growth opportunities
• Attractive benefits including pension plan and EGYM Wellpass

Contact

Apply now and join the Artivion Team. We are looking forward to receiving your application documents in English directly via our online system.

Brian Russo,
T: [phone]

JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.,
Lotzenäcker 23, 72379 Hechingen

www.artivion.com