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Our database has identified the following jobs as matching your search criteria. If you cannot see a job you are interested in, please search again refining your criteria or email us for further help and support.| Title | Clinical Research Associate | ||
|---|---|---|---|
| Role | Clinical Research Associate | Reference | RF/10631 |
| Location | Hertfordshire | Working hours | Full-time |
| Salary | On application | Employment type | Contract / Interim |
| Summary | An exciting opportunity to work within a leading global healthcare company based in Hertfordshire. For over 100 years they have been active in the discovery, development, manufacture and marketing of healthcare solutions. They are seeking an office based Clinical Research Associate in Oncology trials. The role will involve study site management activities related to start up activities, regulatory and CRF compliance, patient enrolment, protocol adherence and data quality for clinical trials and the development and maintenance of investigator relationships. | ||
| Description | Responsibilities: • Conduct pre-study site management activities including contributing to site and investigator selection process • Evaluate site facilities and staff to ensure that the investigative site meets ICH/GCP, local regulatory requirements and protocol • Ensure subject informed consent(s) and protocol are approved by local Ethics Committee(s) and informed consent processes at site are in place as well as all required study start-up documentation • Assist and provide feedback on site issues during site development and negotiation process • Oversee and facilitate Study Start-up Activities • Perform site training and monitoring activities • Ensure the site has appropriate supplies • Design site-level recruitment plan • Perform on and off site monitoring activities in adherence to Protocol, ICH GCP, local regulatory requirements • Verify complete and accurate reporting of SAE • Perform SDV during on-site monitoring • Conduct study site close-out activities This is a fantastic opportunity to work with a world leading Pharmaceutical organisation. | ||
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