Job Title

Position: Central Study CoordinatorLocation: Remote, IndiaEmployment Type: 10 hours per weekIndustry: Clinical Research / Life SciencesLanguages: English and Gujarati About the RoleWe are seeking a detail-oriented and proactive Central Study Coordinator to support the planning, execution, and oversight of clinical research studies. This remote opportunity within India serves as a central operational hub—coordinating study activities, maintaining study documentation, assisting site teams, and ensuring all study processes align with regulatory and sponsor requirements.This role is as a freelancing opportunity only starting immediately and to be completed remotely.Key ResponsibilitiesSupport day-to-day coordination of clinical study operations.Maintain study documentation, trackers, logs, and study management systems.Serve as a central point of communication between study sites, vendors, and internal teams.Assist with study start-up activities, including document collection and site readiness.Track enrollment, site performance metrics, and study timelines.Perform quality checks on study documents to ensure compliance with GCP, SOPs, and regulatory standards.Coordinate study meetings, prepare agendas, and document meeting minutes.Support monitoring activities by assisting with follow-ups, reconciliation tasks, and issue resolution.Contribute to the development and review of study materials such as training guides, manuals, and plans.QualificationsBachelor’s degree in Life Sciences, Nursing, Public Health, or a related field.1 year of experience as a CRA, CTA, or study coordination experience preferred.Strong understanding of Good Clinical Practice (GCP) and clinical research processes.Excellent communication, time-management, and organizational skills.Proficiency with study management systems and Microsoft Office Suite.Ability to work effectively in an on-site, team-oriented environment.