Your Strength
- 1.5-4 years of experience in clinical research or site monitoring
- Proven ability to manage 10-15 clinical study sites from start-up to close-out
- Strong knowledge of ISO 14155, GCP, MDR, FDA, EU, and local regulations
- Skilled in conducting independent on-site and remote monitoring visits
- Strong communication and organizational skills with a proactive mindset
- Ability to mentor and support junior CRAs
- Fluent in English (written and spoken)
- Proficient in Microsoft Office and clinical trial systems (e.g. eTMF, CTMS)
Your Contribution
- Independently plan, conduct, and document site monitoring, initiation, and close-out visits
- Serve as the main contact between the sponsor and investigational sites
- Support site staff with training and issue resolution
- Ensure adherence to protocols and regulatory requirements
- Track progress, follow up on action items, and maintain study records
- Participate in audits, quality checks, and CAPA processes
- Oversee data collection, CRF accuracy, and data clarification
- Assist in study close-out and generate site visit reports
- Support the supervision of clinical trials in collaboration with senior team members
Our Strength
- A mission-driven company focused on improving patient outcomes
- A collaborative, international work environment with high standards
- Opportunities for growth within a strong Clinical Affairs team
- Flexible working conditions and a focus on work-life balance
Contact
JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.,
Lotzenäcker 23, 72379 Hechingen
www.artivion.com
