Clinical Research Coordinator

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: ₹25,799.86 - ₹40,161.70 per month

Benefits:

• Health insurance
• Paid sick time
• Provident Fund

Work Location: In person