Posted on: Mon 27-07-2026

Unique Pharmaceuticals Limited is a pioneer in the pharmaceutical industry in Nigeria. We have been serving the healthcare sector since 1988 through the production & distribution of quality pharmaceutical products, notably I.V. Fluids products manufactured using the innovative and High -Tech manufacturing process known as “Form – Fill – Seal” Technology.

We are recruiting to fill the position below:

Job Title: Pharmacovigilance Data Analyst

Location: Ogun

Employment Type: Full-time

 

Core Responsibilities:

• Data Processing & Case Management: Process Individual Case Safety Reports (ICSRs), Serious Adverse Events (SAEs), and SUSARs in global safety databases.
• Safety Analysis & Signal Detection: Analyze large datasets and clinical trial findings to identify and investigate potential drug safety signals and trends.
• Regulatory Reporting: Draft narrative reports and assist in preparing aggregate safety updates, such as Periodic Benefit-Risk Evaluation Reports (PBRERs) and Development Safety Update Reports (DSURs).
• Engages in pharmacovigilance system master file and risk management system
• Data Quality & Compliance: Perform Quality Control (QC) checks on case data ensuring adherence to ICH E2E, Good Clinical Practice (GCP), and Good Pharmacovigilance Practice (GVP) guidelines.
• Medical Coding: Apply standardized medical terminology (MedDRA, WHODRUG) to adverse events, medical histories, and concomitant medications
• Cross-Functional Collaboration: Communicate safety trends and metrics to medical safety physicians, clinical teams, and regulatory bodies.

Key Qualifications & Skills

• Education: Bachelor’s Degree or higher in Medicine, Pharmacology, Pharmacy, Nursing, Life Sciences, Statistics, or Public Health.
• Technical Software: Proficiency in specialized drug safety systems (e.g., Oracle Argus), coding terminology (e.g., MedDRA, WHODRUG), and data analysis tools (e.g., SAS, R, SQL, or Python).
• Experience: 2 - 4 years of experience in pharmacovigilance, drug safety data analysis, or a clinical research environment.
• Regulatory Knowledge: Solid understanding of ICH (E2A, E2B, E2E), and GVP guidelines.

Application Closing Date

6th August, 2026.

 

Method of Application

Interested and qualified candidates should send their CV to: [email protected] using the Job Title as the subject of the mail.

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