Clinical Research Associate I

Overview

In this role you will support clinical research at the frontline, coordinating with project stakeholders to meet timelines, targets and data quality standards. You will nurture relationships with clinical sites and investigators, while safeguarding subject rights and safety. You will conduct onsite monitoring, assist with study startup and regulatory submissions, and collaborate with cross-functional teams to drive progress and data integrity. This is an opportunity to grow as a clinical research professional within a global team focused on bringing new medicines to patients.

Responsibilities

• Conduct and report onsite monitoring visits
• Involvement in study startup (if applicable)
• Review CRF, perform source data verification and resolve queries
• Manage site communication and relationships
• Serve as point of contact for in-house support services and vendors
• Communicate study progress with 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
• PC skills with MS Word, Excel and PowerPoint
• 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
• MS Word
• MS Excel
• MS PowerPoint

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