Study Coordinator at All India Institute of Medical Sciences (AIIMS) (2026-04 – Present)
- Coordinated clinical research studies in accordance with study protocols, ICH-GCP guidelines, and institutional requirements.
- Screened and enrolled eligible participants by assessing inclusion and exclusion criteria as per the study protocol.
- Conducted the informed consent process and ensured participants fully understood the study before enrollment.
- Scheduled and coordinated patient visits, follow-ups, and study-related procedures.
- Collected, reviewed, and maintained accurate source documentation and study records.
- Recorded, monitored, and reported Adverse Events (AEs) in compliance with protocol and regulatory requirements.
- Performed data entry and data management using electronic Case Report Forms (eCRF), Medidata Rave, and IRT (Interactive Response Technology) systems.
- Ensured timely, accurate, and complete documentation while maintaining data integrity and participant confidentiality.
- Coordinated with Principal Investigators, clinicians, sponsors, and monitors to support the smooth conduct of clinical trials.
Trainee Clinical Research Coordinator at Aakash Healthcare Super Speciality Hospital (2025-11 – 2026-04)
- Coordinate and manage day-to-day operations of clinical trials in accordance with study protocols, ICH-GCP guidelines, and institutional requirements.
- Screen, consent, and enroll eligible study participants; maintain accurate documentation of recruitment activities and subject eligibility.
- Conduct study visits, collect and process biological samples, perform study-related assessments, and ensure timely completion of case report forms (CRFs).
- Maintain essential regulatory documents, including IRB or EC submissions, continuing reviews, protocol amendments, and adverse event reports.
- Serve as primary liaison between investigators, study sponsors, monitors, and clinical staff to facilitate study compliance and resolve protocol
- Ensure participant safety by tracking and reporting adverse events and coordinating follow-up care as required.
- Maintain accurate research data through effective data entry, query resolution, and quality control checks within electronic data capture (EDC) systems.
- Manage investigational product (IP) accountability, including receipt, storage, dispensing, and reconciliation in collaboration with the research pharmacy.
Pharmacist (Assistant Pharmacist) at Park Hospital (2025-07 – 2025-10)
- Responsible for managing the procurement, storage and dispensing of medication.
- Handled over 15+ prescriptions per day including discharge medication.
- Gave instruction to patients on proper use, side effects and how to take the prescribed medicines.
- Organizing the pharmacy, delivering and labelling medications.
- Generating Bills of IPD Or OPD prescription.
Pharmacist (Assistant Pharmacist) at Community Health Center (CHC) Government Hospital Sikandarao (2024-08 – 2024-09)
- Responsible for managing the procurement, storage and dispensing of medication.
- Handle over 15+ prescriptions per day including discharge medication.
- Gave instruction to patients on proper use, side effects and how to take the prescribed medicines.
- Organizing the pharmacy, delivering and labelling medications.
- Generating Bills of IPD Or OPD
