CRA I medical device

Fortrea; Maidenhead; Hybrid; GBP 30,000 - 45,000; Full time

Job summary

Fortrea is seeking a CRA I to join our sponsor-dedicated team in clinical research. This hybrid role involves site monitoring, ensuring compliance with regulatory standards, and developing your career within a collaborative organization focused on medical device studies.

Benefits

Structured career development

Mentorship

Growth opportunities

Qualifications

• Minimum of 1 year of relevant experience (e.g., Site Management, CRA).
• Foundational understanding of regulatory guidelines and clinical trial operations.
• Valid driver's license and willingness to travel.

Responsibilities

• Conduct site monitoring visits to ensure adherence to protocols and GCP requirements.
• Oversee site initiation, monitoring, and close-out visits.
• Track and report Serious Adverse Events (SAEs) as required.

Skills

Communication

Organizational

Problem-solving

Education

University degree in life sciences or related allied health field

Job description

Are you ready to grow your career in clinical research?

Fortrea is hiring a CRA I to join our sponsor-dedicated team. This hybrid role is open to candidates based in or around London, with occasional travel to our client's office in Witney (Oxfordshire). It's an exciting opportunity to work on medical device studies. contributing to innovative research while ensuring compliance with regulatory standards and company SOPs.

Why Join Fortrea?

• Join a global, forward-thinking organization at the forefront of clinical research.
• Play an active role in medical device clinical studies.
• Enjoy structured career development, with progression opportunities across CRA levels.
• Thrive in a collaborative environment that prioritizes mentorship, learning, and growth.

Key Responsibilities:

• Conduct and manage study site monitoring visits to ensure adherence to protocols and regulatory/GCP requirements.
• Oversee all site-related activities, including site initiation, monitoring, and close-out visits.
• Ensure patient safety, data accuracy, and compliance with GCP.
• Assist with feasibility assessments, investigator recruitment, and vendor coordination.
• Track and report Serious Adverse Events (SAEs) as required.

Qualifications:

• University degree in life sciences or a related allied health field.
• Minimum of 1 year of relevant experience (e.g., Site Management, CRA).
• Foundational understanding of regulatory guidelines and clinical trial operations.
• Strong communication, organizational, and problem-solving abilities.
• Valid driver's license and willingness to travel.

Ready to take the next step in your clinical research journey? Apply today and help shape the future of clinical trials at Fortrea!

Learn more about our EEO & Accommodations request here.