Looking to build a career in clinical research jobs in India with flexible working hours? A new opportunity has opened at ProPharma for a Freelance Study Coordinator (Remote, 10 hours/week). This role is ideal for candidates with clinical trial coordination, GCP knowledge, and study documentation experience seeking part-time remote work in the life sciences domain.

This remote clinical research job in India allows professionals to contribute to global studies while maintaining flexibility. If you have experience as a CTA, CRA, or Study Coordinator, this opportunity aligns well with your profile.

Job Overview

• Position: Central Study Coordinator
• Company: ProPharma
• Location: Remote (India)
• Job Type: Freelance / Part-time (10 hours/week)
• Industry: Clinical Research / Life Sciences
• Languages Required: English, Gujarati

Key Responsibilities

As a Freelance Study Coordinator, you will:

• Coordinate day-to-day clinical study operations
• Maintain study documentation, trackers, and logs
• Act as a central communication point between sites, vendors, and teams
• Support study start-up activities and site readiness
• Track patient enrollment, timelines, and performance metrics
• Perform quality checks ensuring compliance with GCP, SOPs, and regulatory standards
• Organize study meetings, prepare agendas, and record minutes
• Assist with monitoring activities, issue resolution, and reconciliation tasks
• Contribute to study materials, manuals, and training documentation

Qualifications & Skills

To qualify for this clinical research coordinator job, candidates should have:

• Bachelor’s degree in Life Sciences, Nursing, or Public Health
• Minimum 1 year experience in:
  • Clinical Trial Assistant (CTA)
  • Clinical Research Associate (CRA)
  • Study Coordinator role
• Strong understanding of Good Clinical Practice (GCP)
• Proficiency in clinical trial processes and documentation
• Excellent communication, organization, and time management skills
• Experience with study management systems and MS Office

Benefits of This Role

• Flexible part-time remote job in clinical research
• Opportunity to work with a global CRO (Contract Research Organization)
• Exposure to end-to-end clinical trial operations
• Skill development in GCP compliance and study coordination
• Ideal for professionals seeking freelance clinical research jobs in India

How to Apply

Application Link