Clinical Research Assistant
1 week ago
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
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