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Clinical Research Associate II, basingstoke
Client:
Artivion EMEA
Location:
Job Category:
Other
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EU work permit required:
Yes
Job Views:
2
Posted:
22.08.2025
Expiry Date:
06.10.2025
Job Description:
At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases, working closely with surgeons worldwide to save lives. We are hiring a Clinical Research Associate II / UK Based / France / Belgium.
Your Responsibilities
* Manage 10–15 clinical study sites from start-up to close-out.
* Conduct independent on-site and remote monitoring 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 supervision of clinical trials with senior team members.
Your Qualifications
* 1.5–4 years of experience in clinical research or site monitoring.
* Proven ability to manage multiple clinical study sites.
* Strong knowledge of ISO 14155, GCP, MDR, FDA, EU, and local regulations.
* Skilled in conducting monitoring visits.
* Excellent communication and organizational skills.
* Fluent in English (written and spoken).
* Proficient in Microsoft Office and clinical trial systems (e.g., eTMF, CTMS).
What We Offer
* A mission-driven company focused on patient outcomes.
* International and collaborative work environment.
* Opportunities for growth within our Clinical Affairs team.
* Flexible working conditions supporting work-life balance.
Application Process
Apply now with your application documents in English via our online system. For inquiries, contact Brian Russo at +41 435 08 39 01.
JOTEC GmbH, a subsidiary of Artivion, Inc.
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