Clinical Research Associate I

Overview

Clinical Research Associate I responsible for onsite monitoring and site/investigator communication to support clinical research timelines, standards, and data quality.

What you'll do

• Conduct and report onsite monitoring visits.
• Perform CRF review, source document verification, and query resolution.
• Manage and handle site communication and coordination.
• Serve as a point of contact for in-house support services and vendors.
• Communicate with internal project teams about study progress.
• Support feasibility research and study startup (if applicable).
• Support the regulatory team with documents for study submissions.

What you'll need

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

Details

• Location: Oxford, England, United Kingdom.