Clinical Research Associate

Kolkata

About the Role

This is a full-time, on-site position supporting the planning, implementation, and monitoring of clinical trials. The role involves coordinating with clinical sites, assisting in study start-up, ensuring accurate data collection and documentation, and tracking study progress.

Key Responsibilities

• Coordinate with clinical sites.
• Assist in study start-up activities.
• Ensure accurate data collection and documentation.
• Track study progress.
• Review case report forms.
• Support site training on study procedures.
• Maintain compliance with ethical guidelines and standard operating procedures.
• Collaborate with clinical operations teams, investigators, and stakeholders.
• Contribute to learner training and mentoring where relevant.

Requirements & Tech Stack

• Clinical trial Protocol development, interpretation, and adherence.
• Skills in site communication, monitoring support, and documentation management.
• Experience or understanding of Clinical Trials, including study phases, regulatory requirements, and ethical guidelines.
• Research skills: data review, data analysis basics, literature search, and report preparation.
• Familiarity with Clinical Operations: study coordination, site management, and SOP-driven processes.
• Knowledge of Good Clinical Practice (GCP) and applicable regulatory standards.
• Strong attention to detail.
• Organizational skills.
• Ability to manage multiple tasks and timelines.
• Effective written and verbal communication skills.
• Ability to work collaboratively with multidisciplinary teams.

Qualifications

• Relevant degree in Life Sciences, Pharmacy, Nursing, Biotechnology, or a related field.
• Prior internship or experience in clinical research or healthcare settings is an advantage.