Clinical Research Associate I

Overview

In this role you drive frontline clinical trial activities and ensure data integrity across sites. You will partner with clinical sites to manage timelines, safety, and regulatory compliance within various therapeutic areas. You will support study start-up, monitoring, data verification, and cross-functional communication to keep projects on track. You contribute to high-quality data and patient safety while growing as a clinical research professional within a collaborative, global team.

Responsibilities

• Conduct and report onsite monitoring visits
• Involve in study start-up (if applicable)
• Perform CRF review, source data verification and query resolution
• Manage site communications and relationships
• Serve as point of contact for in-house support and vendors
• Communicate study progress to internal project teams
• Participate in feasibility research
• Support regulatory team in preparing study submission documents

Key requirements

• College/University degree in Life Sciences or equivalent
• Clinical Research or Medical experience
• Independent on-site monitoring experience in the UK
• MS Word, Excel and PowerPoint skills
• Ability to plan, multitask and work in a dynamic team
• Communication, collaboration, and problem-solving skills
• Ability to travel
• Valid driver’s license

• communication
• collaboration
• problem-solving
• On-site monitoring
• CRF review
• Source data verification

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