Clinical Research Coordinator Responsibilities and Duties
- Coordinate and manage clinical trial activities from initiation to close-out
- Recruit, screen, and enroll study participants according to protocol criteria
- Obtain informed consent and ensure participant understanding
- Schedule and conduct study visits, procedures, and assessments
- Maintain accurate and complete study documentation and records
- Ensure compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines
- Communicate effectively with investigators, sponsors, and regulatory bodies
- Monitor participant safety and report adverse events promptly
- Manage study budgets and supplies as needed
Clinical Research Coordinator Qualifications and Skills
- Strong organizational and time-management abilities
- Excellent communication and interpersonal skills
- Proficiency in Microsoft Office and clinical trial management systems
- Knowledge of clinical research regulations and guidelines
- Attention to detail and problem-solving skills
- Ability to work independently and collaboratively in a team environment
Education and Experience Requirements
- Bachelor's degree in a health-related field (e.g., Nursing, Biology, Public Health)
- Certification as a Clinical Research Coordinator (e.g., ACRP or SOCRA) is a plus
- Current CPR certification may be required
Job Types: Full-time, Permanent, Fresher
Pay: ₹30,799.86 - ₹45,161.70 per month
Benefits:
- Health insurance
- Paid sick time
- Provident Fund
Work Location: In person
