Job Description

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 Requirement

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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: ₹29,799.86 - ₹40,161.70 per month

Benefits:

Health insurance Paid sick time Provident Fund
Work Location: In person