Clinical Research Assistant

Education

• PharmD /Bachelor’s degree in life sciences from HEC / International Approved University

Experience

• 2-3 years

Requisites for the Role

• Fluency in English.
• Strong spoken and written communication skills, including grammatical/technical writing.
• High proficiency with full Microsoft applications

Roles and Responsibilities

• To function as a member of the project team to contribute to the efficient management of trials.
• To negotiate investigator budgets and assist in executing site contracts with support from the legal department.
• To participate in the recruitment of potential Investigators, preparation of Independent Ethics Committee/Independent Regulatory Board (IEC/IRB) submissions, notifications to regulatory authorities, organization of meetings, and other tasks as directed by the Clinical Research Associate – III or Lead Clinical Research Associate/Associate Project Lead/Project Lead.
• To communicate with Investigators and other trial staff, ensuring compliance with protocol requirements, local regulations, ICH-GCP, and DRK Pharma Solutions SOPs.
• To conduct initiation visits, training Investigators and trial staff in the protocol and data collection methods to ensure accurate and complete patient data collection.
• To conduct monitoring visits, ensuring adherence to protocol, accurate data collection, and accountability of investigational products/biological samples/supplies.
• To effectively communicate with site personnel, including the Principal Investigator (PI), and DRK management to address protocol/study deviations and implement corrective actions.
• To update the Clinical Study Management System (CSMS) on time.
• To monitor and update data in an Electronic Data Capture (EDC) system according to study guidelines.

Deadline To Apply

November 16, 2025

Job Type: Full-time

Pay: From Rs75,000.00 per month

Work Location: In person