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Senior Clinical Research Associate (Senior CRA), Slough
Client: EPM Scientific
Location: Slough, United Kingdom
Job Category: Other
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EU work permit required: Yes
Job Views: 3
Posted: 22.08.2025
Expiry Date: 06.10.2025
Job Description:
We're currently partnering with a leading international pharmaceutical company to recruit a Senior Clinical Research Associate.
Location: West London
Hybrid: Twice a week in office
Job Summary
* Feasibility assessments/visit evaluations for clinical trials.
* Site setup for commercial distribution and for clinical trials.
* Study management.
* Site management investigating, following up, and escalating site issues as needed.
* Conduct remote and on-site visits in accordance with protocols, GxP guidelines, applicable local and international regulations, and company SOPs to ensure subjects' rights, well-being, and data reliability, ensuring audit readiness.
* Relationship management with site staff.
* Assistance with pharmacovigilance, safety reporting management.
* In-house/on-site document quality management.
Responsibilities
* Management of studies.
* Site evaluation and setup for commercial distribution including site training.
* Maintenance of contacts with sites for commercial distribution and sites involved in clinical trials.
* Collection of essential documents according to ICH-GCP, GVP, and applicable regulations.
* Monitoring of data collection and pharmacovigilance/safety reporting at the sites where a study is conducted.
* Site setup, training, initiation, close-out, and management (including monitoring) of studies.
* Site management including site payment process and reconciliation.
* Study/clinical trial status tracking, QC, and progress updates to the team.
* Prepare or review site visit reports.
* Participation in investigator meetings and other meetings as necessary.
* Attendance and representation at conferences as applicable.
* Contribution to other tasks such as creation of newsletters as directed.
* Assist with inspections/audits as required.
* Contribute to the preparation of CSR/publications, informed consents, protocols, and guidelines, sharing ideas with study members.
* Prepare documents such as informed consent, monitoring plans, and study operating manual for studies.
* Assist in creating project-specific training for junior members and sites.
* Identify areas for potential process improvements and bring these to the attention of the Clinical Operations Manager.
* Preparation of literature reviews and searches.
* Contribution to scientific discussions regarding therapeutic areas, treatments, study endpoints, and investigational medicinal products.
Qualifications/Experience
* Graduate qualifications in Biological Sciences, Nursing, Pharmacy, or related discipline.
* Post-graduate qualifications desirable.
* At least 4 years proven experience as a CRA.
* On-site experience.
* Working knowledge of ICH GCP guidelines.
* Proven experience in managing clinical trials/projects.
What's on Offer
* A competitive salary with benefits.
* The chance to contribute and be part of a team whose work directly benefits healthcare and strives to improve people's lives.
* A hands-on opportunity to gain high commercial exposure.
* The chance to work alongside world-leading scientific experts.
* Work with highly talented and dedicated colleagues in a fast-growing company focusing on cutting-edge science and commercial delivery.
Interested in making a difference?
Apply now or reach out to learn more about this exciting opportunity!
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