OverviewI 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.ResponsibilitiesOversee regulatory compliance for clinical trials in accordance with local and international regulationsCoordinate with regulatory authorities and ethics committees for approvals and submissionsEnsure documentation and reporting are in line with regulatory requirementsConduct site visits to assess regulatory compliance and provide support and guidance to site staffCollaborate with cross-functional teams to ensure regulatory milestones are achievedQualificationsBachelor's degree in a scientific or healthcare disciplineProven experience as a Clinical Research Associate in regulatory activitiesIn-depth knowledge of regulatory requirements for clinical trials in SpainStrong understanding of ICH-GCP guidelines and other relevant regulationsExcellent communication and interpersonal skillsAbility to work independently and manage time effectivelyDay-to-DayAs 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.BenefitsOpportunity to work on a part-time basis with a flexible scheduleGain valuable experience in regulatory activities within clinical researchCollaborate with a dynamic and supportive teamCompetitive compensation package
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