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Clinical Research Associate - reduced travel

Reading, Berkshire💼 Full-time🗓 2026-05-20 → 2026-07-29

Core

Lead clinical trial monitoring tasks ensuring adherence to protocols, regulatory requirements, and GCP standards while managing site performance and data integrity.

Role type

Senior Clinical Research Associate (SSU)

Builds

Clinical trial execution and data collection

Domain

Healthcare / Clinical Research

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

Clinical trial monitoring, site management, data integrity, regulatory compliance (GCP), project management, clinical trial software proficiency

Preferred skills

SSV and submission experience, ability to guide others, problem-solving

Responsibilities

Monitor clinical trial sites for protocol and regulatory adherence, conduct site visits to assess performance and resolve issues, collaborate on data collection and reporting, provide training to site staff and CRAs, manage multiple sites and projects simultaneously

Seniority

Senior, hands-on IC

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