We are looking for CRA to take on a range of dynamic projects across multiple therapeutic areas. My client understands everyone has different career ambitions which is why they offer personal development plans that are tailored to your passions.
Our offer: Work with a Global CRO where creating a team of CRAs to go above and beyond just monitoring duties is at the forefront of the company’s focus. The role will allow you to develop your strengths and work in the aspects of clinical trials that interest you.
If you are looking to develop your career within healthcare and life sciences, then we really want to hear from you!
•Perform feasibility studies for potential sites as requested
•Conduct pre-study, study initiation and interim monitoring visits in adherence to the protocol requirements
•Function in the role of Lead CRA for global studies, coordinating CRAs
•Develop Clinical Monitoring Plan as requested
•Conduct site visit trip report review and provide feedback and edits
• 18 months independent monitoring experience
• Good knowledge of ICH-GCP and relevant regulations
• Excellent communication skills
• Strong attention to detail
Full job description and company details are available upon application, apply below. This position is being dealt with by Jack Lynch a at Meet, please call +44203 019 3998. You can also e-mail us directly at firstname.lastname@example.org to discuss in confidence.
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