Job Title

Position: Central Study Coordinator Location: Remote, India Employment Type: 10 hours per week Industry: Clinical Research / Life Sciences Languages: English and Gujarati About the Role We 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 Responsibilities - Support 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. Qualifications - Bachelor'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.