Our client, a prestigious London University, is currently seeking a dynamic individual to join them as a temporary Clinical Trials Monitor. The position is 35 hours per week, for 3 months in the first instance, based in Whitechapel.
Key Responsibilities for this role include:
- Completing all on-site monitoring as per the approved trial monitoring plan.
- Completing laboratory and pharmacy visits, providing detailed reports on your findings.
- Providing written reports after each visit to document your visits including your findings, conclusions, and actions taken or recommended to secure compliance.
- Maintaining regular and effective communication with site staff to ensure that any non-compliances or data errors are reported and addressed in a timely manner.
- Regularly monitor the Trial Master File to ensure that all essential documents are present, accurate and maintained.
- Attending Trial Management Meetings and providing accurate, detailed updates where required.
To be considered for this position, you should possess:
- Previous experience in a similar role, preferably within a higher education setting.
- Demonstrable, strong experience in monitoring or coordinating clinical research studies.
- Experience of writing up detailed reports for research projects.
- Excellent communication and organisational skills with a keen attention to detail.
- Proficiency in using various IT systems.
- Ability to work proactively and independently.
- Analytical skills and ability to problem solve and make quick decisions.
The position aims to start as soon as possible, requiring candidates to be available immediately or have a short notice period to be considered.
If you would like to be considered for this opportunity, kindly express your interest by submitting your CV in Word format.
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