Clinical Research Associate I
Core
Frontline communication with project stakeholders to ensure timelines, targets, and standards of clinical research projects across various therapeutic indications.
Role type
Junior Clinical Research Associate (IC)
Builds
Clinical research projects ensuring subject safety, data compliance, and study execution
Domain
Healthcare / Clinical Trials
Required skills
On-site monitoring, Source document verification, CRF review, Query resolution, Site management, Feasibility research, Regulatory document preparation, PC skills (Word, Excel, PowerPoint), Planning and multitasking
Preferred skills
Independent on-site monitoring experience in the UK, Valid driver's license, Ability to travel
Responsibilities
Conduct and report onsite monitoring visits, Perform CRF review and source document verification, Manage site communication, Support regulatory team in preparing submission documents, Participate in feasibility research
Seniority
Junior, hands-on IC