Clinical Research Coordinators (Interns / Freshers)

Pre-Trial Responsibilities:
- Identify and qualify potential clinical trial sites and investigators.
- Ensure trial sites are equipped with necessary materials and equipment.
- Train site staff on study procedures and data collection methods.
- Maintain study manuals and documentation.

Monitoring Responsibilities:
- Conduct regular site visits to monitor progress and adherence to protocols.
- Review case report forms and data for accuracy and completeness.
- Address safety concerns and protocol deviations.
- Report findings to sponsors and regulatory authorities.

Post-Trial Responsibilities:
- Assist with data analysis and study close-out activities.
- Prepare final study reports and presentations.
- Support regulatory submission processes.

Additional Responsibilities:




- Manage study budgets and timelines.
- Coordinate with ethics committees and regulatory agencies.
- Provide scientific and technical support to study teams.
- Participate in training and development programs.

Qualifications:
- Open to Interns / Freshers.
- Bachelor's degree in life sciences, nursing, or a related field.
- Valuable understanding of Good Clinical Practice (GCP) guidelines and regulations.
- Strong communication, interpersonal, and organizational skills.
- Keen attention to detail and ability to multitask.
- Willingness to travel frequently and independently.

Pay: From ₹35,000.00 per month

Work Location: In person

📌 Clinical Research Coordinator (Velachery)
🏢 Clinogenesis Research Institute
📍 Velachery