Clinical Research Associate
Clinical Research Associate
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Job Description
Job Description
Overview
I am seeking a professional and experienced Clinical Research Associate to join the team in Spain for a respected Sponsor company I am partnered with. This is a freelance parttime position with a 0.5 FTE commitment for a 12month 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 crossfunctional teams to ensure regulatory milestones are achieved
Qualifications
- Bachelors degree in a scientific or healthcare discipline
- Proven experience as a Clinical Research Associate in regulatory activities
- Indepth knowledge of regulatory requirements for clinical trials in Spain
- Strong understanding of ICHGCP guidelines and other relevant regulations
- Excellent communication and interpersonal skills
- Ability to work independently and manage time effectively
DaytoDay
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 parttime basis with a flexible schedule
- Gain valuable experience in regulatory activities within clinical research
- Collaborate with a dynamic and supportive team
- Competitive compensation package
Required Experience:
IC
Employment Type
Full-Time
