Clinical Research Associate (CRA)
Remote with regular UK travel
Temporary 6-9 months
SRG is proud to be working with a leading cancer research organisation to support them on their hunt for a proactive Clinical Research Associate (CRA) to monitor clinical trials across sites throughout the UK. This role focuses on ensuring trials are delivered to a high standard, in compliance with ICH-GCP and applicable UK/EU regulations, while building strong site relationships.
Key Responsibilities:
- Organise, conduct and document site initiation visits (SIVs) and routine monitoring visits in line with SOPs and monitoring guidelines.
- Support Trial Master File (TMF), Investigator Trial File (ITF) and Pharmacy File set-up, maintenance, review and archiving.
- Support site selection activities including feasibility questionnaires and pre-study visits.
- Provide trial-specific training to site staff and ongoing support to ensure timely reporting of serious adverse events (SAEs).
- Ensure sites comply with protocol, SOPs and regulatory requirements; manage deviations and escalate issues/serious breaches as needed.
- Conduct pharmacy visits and ensure investigational medicinal product (IMP) is stored, handled, dispensed and reconciled appropriately.
- Work with Data Management to support data quality and timelines (e.g., query resolution, patient/database milestones).
- Contribute to process improvements and support onboarding/training of new team members where required.
Key Requirements:
- Life sciences degree or equivalent nursing qualification/experience.
- Strong working knowledge of ICH-GCP, clinical trial methodology and relevant UK/EU regulations.
- Able to work independently across multi-centre studies; excellent organisation and time management.
- Strong written and verbal communication skills; confident building relationships with site teams and internal stakeholders.
- Proficient in Microsoft Office (Word, Excel, PowerPoint).
- Willingness to travel regularly across the UK.
- Oncology and/or early phase (non-healthy volunteer) monitoring experience.
- Experience with EDC systems and/or eTMF platforms.
Apply now by attaching your CV in Word, or contact Paige Keenan for further information about this new role: [email protected]