Narmeen Tariq

ACRP-CP certified Clinical Research Professional with a PharmD degree and over 4 years of experience supporting Phase I–III clinical trials, project coordination, regulatory compliance and clinical operations within healthcare and research environments. Experienced in coordinating multi-site studies, maintaining TMFs/eTMFs, supporting study start-up and closeout activities and collaborating with sponsors, investigators, CROs, and interdisciplinary teams.

Clinical Research Data Coordinator at Metrics Research (DM Clinical Research) (2023-02 – 2025-02)

• Supported pharmacovigilance and clinical safety activities for multiple industry-sponsored clinical studies involving over 150+ participants, ensuring accurate adverse event documentation and safety tracking
• Supported clinical trial start-up activities including preparation of regulatory documentation, ethics submissions, protocol amendments, investigator site files, contributing to successful study activations and audit.
• Assisted with collection, review, and reconciliation of adverse event and serious adverse event (SAE) documentation, contributing to timely case reporting and improved safety documentation accuracy by 30%.
• Assisted with study tracking, milestone reporting, recruitment coordination, patient scheduling and investigational product accountability while effectively managing multiple concurrent studies.
• Collaborated with investigators, sponsors, CROs, and multidisciplinary teams to support safety reporting workflows, protocol amendments, training coordination, and study milestone tracking.

Research Pharmacist at Aga Khan Hospital and Medical College Foundation (2021-07 – 2023-02)

• Supported pharmacovigilance activities by documenting, reviewing, and escalating adverse events and serious adverse events, ensuring timely reporting and compliance with institutional and regulatory requirements.
• Conducted clinical literature reviews and supported preparation of scientific summaries, patient information materials, and study-related documentation to ensure evidence-based clinical decision support.
• Prepared and submitted regulatory documentation, including ethics applications, safety updates, and protocol amendments, ensuring 100% compliance with GCP and research ethics standards.
• Supported two successful DRAP regulatory inspections and sponsor audits by maintaining audit ready documentation, resolving compliance findings proactively and coordinating corrective actions.
• Collaborated with sponsors, investigators and healthcare professionals to resolve protocol deviations, optimize study workflows and improve operational coordination, contributing to an 15% reduction in study delays.

Pharm-D in Pharmacy – Dow University of Health Sciences (2013-01 – 2018-01)