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Clinical Research Associate (CRA, Slough)
Client:
EPM Scientific
Location:
Slough, United Kingdom
Job Category:
Other
EU work permit required: Yes
Job Views:
2
Posted:
22.08.2025
Expiry Date:
06.10.2025
Job Description:
We're currently partnering with a leading international pharmaceutical company to recruit a Junior CRA.
Location: West London
Hybrid: Twice a week in office
Description of the Role:
* Site evaluation and setup for commercial distribution including training of dosing in collaboration with the Clinical Project Manager or designee
* Maintenance of contacts with sites for commercial distribution and sites involved in clinical trials
* Collection of essential documents according to ICH-GCP E6 (R2) and applicable regulations
* Monitoring of data collection and pharmacovigilance/safety reporting at sites conducting post-authorization studies
* Site setup, initiation, close-out, and management (including monitoring) of clinical and post-authorization studies as needed
* Site management including supplies and payments
* Tracking study/clinical trial status and updating the team
* EC/IRB and regulatory submissions
* Participation in investigator meetings and other meetings
* Attendance at conferences as applicable
* Contribution to newsletters and other tasks as directed
* Assist with audits as required
* Contribute to initiatives and process improvements
* Contribute to Literature Reviews
Key Result Areas:
* Feasibility assessments and visit evaluations for clinical and post-authorization studies
* Site setup for commercial distribution and clinical trials
* Site management: investigating, following up, and escalating issues
* Delivering data accuracy through CRF review and monitoring to ensure patient safety and compliance
* Assistance with pharmacovigilance and safety reporting
* Document quality management (trial master file, investigator site file)
Qualifications/Experience:
* Graduate qualifications in Biological Sciences, Nursing, Pharmacy, or related discipline
* Post-graduate qualifications desirable
* At least 2 years proven experience as a CRA
* Working knowledge of ICH GCP guidelines
* On-site experience
* Proven experience in managing clinical trials/projects
What's on Offer:
* A competitive salary with benefits
* The opportunity to contribute to healthcare and improve lives
* Hands-on experience with high commercial exposure
* Work alongside scientific experts
* Join a fast-growing, innovative company
Interested in making a difference? Apply now or reach out to learn more about this exciting opportunity!
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