Clinical Research Associate

Roles & Responsibilities
• Conduct site initiation, routine monitoring, and close-out visits as per protocol and GCP
• Ensure site compliance with study protocol, SOPs, and regulatory guidelines
• Build and maintain effective relationships with investigators, coordinators, and site staff
• Perform source data verification (SDV) and ensure data accuracy and integrity
• Identify, document, and follow up on data queries and monitoring findings
• Support preparation and submission of regulatory documents to ECs and authorities
• Monitor and report adverse events and ensure timely safety reporting
• Collaborate with data management teams for accurate data collection and validation
• Provide training and ongoing support to site staff throughout the study lifecycle
• Act as a key point of contact between sites and internal cross-functional teams

Qualification
• Bachelor’s degree in Life Sciences or a related field

Experience
• Minimum 3 years of experience as a Clinical Research Associate
• Hands-on experience in site management and clinical trial monitoring
• Proven exposure to end-to-end clinical trial activities

Skills
• Strong knowledge of ICH-GCP and regulatory requirements
• Excellent verbal and written communication skills
• Strong organizational and time management abilities
• High attention to detail and problem-solving skills
• Ability to work independently and within cross-functional teams
• Willingness to travel to investigative sites as required

About the Organization
MS Clinical Research Pvt Ltd is a leading clinical research organization committed to advancing scientific innovation through high-quality clinical trials. The company focuses on regulatory-compliant research practices to support the development of safe and effective medical solutions that improve healthcare outcomes.