Clinical Research Associate

Roles & Responsibilities
• Monitor and oversee clinical trials at investigational sites
• Conduct site initiation, routine monitoring, and close-out visits
• Ensure compliance with study protocols, ICH-GCP, and regulatory guidelines
• Track clinical operations timelines and study progress
• Verify source documents and ensure data accuracy and integrity
• Prepare monitoring visit reports and maintain essential trial documentation
• Coordinate with investigators, site staff, and internal cross-functional teams
• Ensure proper maintenance of Trial Master File (TMF) documents
• Identify protocol deviations and support corrective and preventive actions (CAPA)
• Support audit and inspection readiness activities

Qualification
• Bachelor’s Degree in Life Sciences, Pharmacy, or related field

Experience
• Prior experience in clinical research industry (preferred but not mandatory)
• Understanding of clinical trial processes and clinical operations
• Exposure to regulatory requirements and compliance standards

Skills
• Strong knowledge of ICH-GCP guidelines
• Attention to detail and high documentation accuracy
• Good organizational and time management skills
• Effective communication and stakeholder coordination
• Ability to work independently and on-site

About the Organization
Eccentric Clinical Research (ECR) is a comprehensive clinical research service provider supporting pharmaceutical, nutraceutical, cosmetic, herbal, and medical device companies. The organization delivers customized research solutions while maintaining high regulatory, ethical, and quality standards across clinical development projects.