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Freelancer-Study Coordinator- 10 hours per week

Location

India

JobType

part-time

About the job

Info This job is sourced from a job board

About the role

ProPharma

Website: propharmagroup.com
Job details:

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.

Click on Apply to know more.

Skills

compliance
GCP