Clinical Research Associate

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, 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 Spain

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

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