Clinical Research Coordinator
2 days ago
**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.
- Good 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
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