Clinical Research Associate

About the Role

We are looking for motivated freshers to support clinical trial activities, study documentation, and coordination while ensuring compliance with clinical research guidelines.

Key Responsibilities

• Assist with clinical trial coordination and study documentation.
• Maintain essential clinical trial documents and records.
• Support clinical study monitoring and site coordination activities.
• Ensure compliance with GCP guidelines, study protocols, and SOPs.
• Assist in data review, report preparation, and follow-up activities.
• Coordinate with investigators, study teams, and other stakeholders.

Requirements

• B.Pharm, M.Pharm, B.Sc./M.Sc. Life Sciences, Biotechnology, Microbiology, Nursing, or a related qualification.
• Basic knowledge of clinical research, clinical trials, and GCP.
• Good communication, documentation, and organizational skills.
• Attention to detail and willingness to learn.