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 Valuable 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
Robust 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 workplace

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

📌 Clinical Research Coordinator Nashik
🏢 Statistical Insights
📍 Nashik