Contractor Senior Clinical Research Associate - Contractor - UK
Core
Conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol adherence and data integrity for clinical trials.
Role type
Senior Clinical Research Associate (CRA)
Builds
Clinical trial data and compliance documentation
Domain
Clinical Research / Healthcare
Deliverable
client delivery
Required skills
Site management, protocol adherence monitoring, source document verification, CRF review, TMF management, regulatory submission support, data query resolution, patient safety assessment, informed consent review, mentoring junior staff
Preferred skills
Experience in Neuroscience, Oncology, Cardiovascular, Metabolic, or Rare Diseases therapeutic areas
Responsibilities
Conduct site qualification, initiation, interim monitoring, and study close-out visits; Document site visit findings via written reports; Assess, monitor, and train study site staff on protocol adherence; Review study subject safety information and informed consent; Conduct source document verification for compliance and data veracity; Review CRFs and assist with data query resolution; Provide updates for site documentation in the Trial Master File; Ensure site compliance with IP receipt and accountability; Conduct accompanied site visits for assessment or training of other CRAs