Clinical Research Associate III (m/f/d)

Jotec GmbH Jobportal
Hechingen

Kaufmännische Berufe (Sonstige)
Publiziert: 13.01.2026

Clinical Research Associate III (m/f/d), 1. Bild

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

Clinical 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