cra jobs in Edinburgh

Hlx Life Sciences is seeking a Freelance CRA for a part-time UK-based assignment. You will monitor sites across a global clinical trial, initiate and perform site visits, manage relationships with investigators, and ensure data quality and regulatory compliance.French and English fluency is required, with willingness to travel and experience in multinational...

Role: OT Cyber Security Senior ManagerLocation: UK (typically 1day per week in our London office, with additional client site visits as needed).Level: Senior ManagerSalary: Competitive Salary & Package (Dependent on Experience)Please Note: Any offer of employment is subject to satisfactory BPSS and SC security clearance which requires 5 years continuous UK...

Freelance CRA – UK | French & English Speaking I’m currently supporting a CRO looking to bring an experienced Freelance CRA onto a part-time, sponsor-dedicated project. The CRA will be based in the UK and work closely with both the CRO and sponsor teams, supporting sites as part of a global clinical trial. We’re particularly interested in CRAs who have...

Discover International is seeking a Clinical Research Coordinator to support multi-site trials across oncology, cardiovascular, and rare disease indications in partnership with a UK CRO.You will coordinate site start-up and maintain TMF per ICH-GCP, liaise with investigators, sponsors, and internal teams to meet milestones, assist CRAs with scheduling and...

Discover International is partnered with a UK-based CRO who are seeking a Clinical Research Coordinator to support multi-site clinical trials across oncology, cardiovascular, and rare disease indications.Key ResponsibilitiesCoordinate site start-up and maintain Trial Master Files (TMF) per ICH-GCPLiaise with investigator sites, sponsors, and internal teams...

Discover International is partnered with a UK-based CRO is seeking a Clinical Trial Manager to lead the operational delivery of Phase I–IV clinical trials for pharmaceutical and biotech sponsors, managing cross-functional teams and study timelines from start-up through close-out.Key ResponsibilitiesOwn end-to-end trial management for assigned studies,...

Responsibilities (a) Site management Study site selection, initiation (SIV) and clinical monitoring. Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to...

This range is provided by Alimentiv. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range In this role you will be providing unbiased medical guidance to clinical sites and internal and external study operations teams. You will also be providing therapeutic and compound training, medical...