Published 2026-04-19
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.
