Summary: The Clinical Research Associate (CRA) role involves supporting and monitoring clinical studies related to medical devices, ensuring compliance with protocols and maintaining relationships with healthcare professionals. The position requires training healthcare staff on device usage and troubleshooting basic technical issues. This is a 12-month fixed-term contract based in Witney, England, with occasional travel to study sites. The ideal candidate will possess strong communication skills and a detail-oriented approach to clinical research.

Key Responsibilities:

• Act as a monitor for clinical studies, ensuring adherence to protocols and regulatory requirements.
• Build and maintain strong relationships with nurses, doctors, and healthcare staff at study sites, including hospitals and GP practices.
• Train healthcare professionals on the use of medical devices involved in the study.
• Set up and configure laptops to ensure smooth data transfer and troubleshoot basic technical issues.
• Ensure all study documentation is accurate, complete, and in compliance with clinical research protocols.
• Follow detailed procedures and apply them effectively in a real-world setting.
• Remain calm under pressure and troubleshoot issues as they arise.
• Travel to study sites when required (maximum once per week but may vary).

Key Skills:

• Previous experience in a clinical research role, preferably with medical devices.
• Strong communication and interpersonal skills to liaise effectively with healthcare professionals.
• Ability to follow protocols and procedures accurately.
• Problem-solving mindset with a calm and methodical approach to challenges.
• Comfortable with basic IT tasks, including laptop setup and data transfer troubleshooting.
• Experience with clinical study monitoring and compliance is an advantage.

Salary (Rate): undetermined

City: Witney

Country: United Kingdom

Working Arrangements: on-site

IR35 Status: fixed-term

Seniority Level: Mid-Level

Industry: Other