Cra I Medical Device
Maidenhead, ENG, GB, United Kingdom
Job Description
Are you ready to grow your career in clinical research?
Fortrea
is hiring aCRA I
to join oursponsor-dedicated
team. This hybrid role is open to candidates based in or aroundLondon
, with occasional travel to our client's office inWitney (Oxfordshire)
. It's an exciting opportunity to work onmedical 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.
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Job Detail
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Job IdJD3215372
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IndustryNot mentioned
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Total Positions1
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Job Type:Contract
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Salary:Not mentioned
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Employment StatusPermanent
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Job LocationMaidenhead, ENG, GB, United Kingdom
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EducationNot mentioned