CRA I medical device

PharmiWeb.jobs: Global Life Science Jobs; Maidenhead; Hybrid; GBP 30,000 - 40,000; Full time

Job summary

Join a leading organization in clinical research as a CRA I focusing on medical device studies. This hybrid role, based in and around Maidenhead, offers growth opportunities and structured career development. Be part of a collaborative team that ensures protocol adherence and patient safety while contributing to innovative research efforts.

Benefits

Career development opportunities

Collaborative work environment

Mentorship and learning

Qualifications

• Minimum 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 and manage study site monitoring visits.
• Oversee site-related activities including initiation and monitoring.
• 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

Join to apply for the CRA I medical device role at PharmiWeb.jobs: Global Life Science Jobs

3 days ago Be among the first 25 applicants

Join to apply for the CRA I medical device role at PharmiWeb.jobs: Global Life Science Jobs

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 .

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Staffing and Recruiting

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