Rashmi .

Enthusiastic and dedicated research professional familiar with clinical trial protocols, informed consent process, and regulatory guidelines including GCP. Strong organizational and communication skills with the ability to manage study documentation and coordinate with investigation and study teams. Committed to maintaining data integrity and supporting high–quality research.

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

M. Pharm in Pharmacology – KDC College of Pharmacy Barari Mathura

B. Pharm in Pharmacy – Maya Group of Pharmacy Sokhana Hathras (2021 – 2025)