Clinical Research Associate I
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Job Description
Clinical Research Associate conducting onsite monitoring, site management, and regulatory support for a global medical research company. Ensuring participant safety, data quality, and study timelines across therapeutic indications.
Responsibilities:
- Work on the frontline of communication with project stakeholders
- Ensure timelines, targets and standards of clinical research projects across therapeutic indications
- Build and maintain relationships with clinical sites and investigators
- Focus on subjects’ rights, safety and well-being and quality of data compliance
- Conduct and report all types of onsite monitoring visits
- Participate in study startup, if applicable
- Perform CRF review, source document verification and query resolution
- Manage site communication
- Serve as a point of contact for in-house support services and vendors
- Communicate with internal project teams regarding study progress
- Participate in feasibility research
- Support the regulatory team in preparing documents for study submissions
Requirements:
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- 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 environment
- Communication, collaboration, and problem-solving skills
- Ability to travel
- Valid driver’s license
Benefits:
- Employees can work remotely
- Support from a knowledgeable and professional team
- Opportunity to develop a variety of skills
- Career progression with the company
- Contribution to full-scale challenging projects
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