Clinical Research Associate

Roles and Responsibilities

• Provide support for clinical trial activities under direct supervision.
• Assist in organizing and maintaining trial-related files and regulatory binders.
• Support CRC-I/CRC-II in coordinating patient visits and follow-ups.
• Perform data entry into CRFs/EDC systems as instructed.
• Prepare visit reminders and follow-up calls under guidance.
• Maintain inventory of study-related supplies and kits.
• Observe and learn to assist with informed consent and participant communication.
• Attend training sessions and assist with basic documentation during site initiation and monitoring visits.

Requisites for the Role

• High proficiency with full Microsoft applications
• Strong spoken and written communication skills to include grammatical/technical writing
• Good Report Writing Skills

Education: Only Bachelors or Masters in Pharm D

Experience: Minimum 1 to 3 years of relevant experience.

Job Type: Full-time

Pay: From Rs65,000.00 per month

Work Location: In person