About
Detail-oriented B.Sc. Life Sciences graduate with postgraduate diploma training in Clinical Research and Pharmacovigilance. Has practical academic exposure to ICSR workflows, regulatory documentation, quality reviews, and medical coding concepts, and is targeting entry-level roles in drug safety, medical coding, or clinical research coordination.
Education
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2026
Post Graduate Diploma in Clinical Research & PharmacovigilanceCPA Institute of Pharmaceutical & Life SciencesClinical Research & Pharmacovigilance · Jul 2026
- 2024
Skills
<3 months
<3 months Just getting started - under three months. This is also what shows when a level has not been set.
Tools / apps / platforms
<3 months
<3 months Just getting started - under three months. This is also what shows when a level has not been set.
Microsoft Word
Microsoft Excel
Microsoft PowerPoint
Projects
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Therapeutic Case Study: Wegovy (Semaglutide)Scientific review, pharmacovigilance surveillance
Technical seminar and scientific review synthesizing clinical efficacy and safety data from the STEP trial program and discussing post-marketing surveillance and risk mitigation.
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Pharmacovigilance & Quality Documentation PracticumICSR processing, safety narrative drafting, APQR, RCA, CAPA, SOP drafting, product monograph development
Academic hands-on project involving simulated adverse event reports, quality review analysis, root cause analysis, CAPA planning, SOP formulation, and product monograph preparation.
Courses & certifications
- Certificate in Good Clinical Practice (ICH-GCP E6 R2) · Verified understanding of clinical trial ethics, investigator duties, and trial integrity · 2026