Clinical Research Associate

Roles & Responsibilities

• Monitor clinical trial activities in accordance with protocol, ICH-GCP, and regulatory guidelines
• Ensure subject safety, data integrity, and regulatory compliance
• Coordinate with investigators, site staff, sponsors, and cross-functional teams
• Review essential documents, CRFs, and clinical trial data
• Support site initiation, monitoring, and close-out activities
• Ensure proper documentation and timely reporting of trial progress

Qualification

• Clinical Research

Experience

• 1–5 years of experience as a Clinical Research Associate

Skills

• Knowledge of clinical research and pharmacovigilance concepts
• Good understanding of GCP, ICH guidelines, and regulatory requirements
• Strong communication and documentation skills
• Willingness to learn and adapt in a regulated clinical research environment

About the Organisation

Pharmazone is a growing organization in the pharmaceutical and clinical research domain, offering opportunities in clinical trials and pharmacovigilance. The company focuses on structured learning, hands-on exposure, and career growth for life sciences professionals seeking to build a strong foundation in clinical research.