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Overview
I am seeking a professional and experienced Clinical Research Associate to join the team in the UK or a respected Sponsor company I am partnered with. This is a freelance, part-time position with a 0.5 FTE commitment for a 12-month duration. The successful candidate will be responsible for regulatory activities related to clinical trials.
Responsibilities
Oversee regulatory compliance for clinical trials in accordance with local and international regulations
Coordinate with regulatory authorities and ethics committees for approvals and submissions
Ensure documentation and reporting are in line with regulatory requirements
Conduct site visits to assess regulatory compliance and provide support and guidance to site staff
Collaborate with cross-functional teams to ensure regulatory milestones are achieved
Qualifications
Bachelor's degree in a scientific or healthcare discipline
Proven experience as a Clinical Research Associate in regulatory activities
In-depth knowledge of regulatory requirements for clinical trials in the UK
Strong understanding of ICH-GCP guidelines and other relevant regulations
Excellent communication and interpersonal skills
Ability to work independently and manage time effectively
Day-to-Day
As a Clinical Research Associate, you will be responsible for ensuring regulatory compliance throughout the lifecycle of clinical trials. This will involve liaising with regulatory authorities, conducting site visits, and maintaining accurate documentation to support regulatory submissions.
Benefits
Opportunity to work on a part-time basis with a flexible schedule
Gain valuable experience in regulatory activities within clinical research
Collaborate with a dynamic and supportive team
Competitive compensation package
Additional Information
Seniority level: Mid-Senior level
Employment type: Part-time
Job function: Research, Analyst, and Information Technology
Industries: Staffing and Recruiting
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