Pharmacovigilance Case Processing SME | Argus/Veeva | ₱30,000 Joining Bonus

Private Advertiser; Taguig; On-site; PHP 360,000 - 520,000; Full time

Benefits offered by this job

Joining bonus

Job summary

Private Advertiser seeks a Pharmacovigilance Case Processing SME to join a global pharmacovigilance team focused on patient safety and regulatory compliance.

You will manage safety cases, adverse event reporting, and data quality activities using Argus and Veeva Safety while supporting global drug safety operations.

Qualifications

• Experience in Pharmacovigilance/Drug Safety
• Proficient in processing and reviewing IC SR s
• Hands-on with Argus Safety, Oracle Argus, Veeva Safety

Responsibilities

• Process, review, and manage ICSRs in line with global standards.
• Adverse event intake, data entry, case triage, and processing.
• MedDRA coding, product coding, and case assessments with accuracy.

Skills

Pharmacovigilance

ICSR processing

MedDRA coding

Data quality

Safety narrative writing

Regulatory compliance

Education

Pharmacy

Nursing

Medical Technology

Medical Laboratory Science

Biomedical Science

Molecular Biology

Pharmaceutical Chemistry

Life Sciences/Healthcare

Tools

Argus Safety

Oracle Argus

Veeva Safety

Job description

₱30,000 Joining Bonus*

Terms and conditions apply.

Join a Global Pharmacovigilance Team Driving Patient Safety

Join a global Pharmacovigilance team dedicated to advancing patient safety and regulatory compliance. As a Pharmacovigilance Case Processing SME, you'll manage safety cases, adverse event reporting, and data quality activities using Argus and Veeva while supporting global drug safety operations.

Key Responsibilities

• Process, review, and manage Individual Case Safety Reports (ICSRs) in accordance with global pharmacovigilance standards.

• Perform adverse event intake, data entry, case triage, and case processing activities.

• Conduct MedDRA coding, product coding, and case assessments while ensuring accuracy and compliance.

• Prepare and maintain high-quality safety narratives and case documentation.

• Perform quality review and quality control activities to ensure data integrity and regulatory compliance.

• Manage safety workflows, case routing, and case lifecycle activities within safety databases.

• Maintain accurate and complete documentation within Argus, Veeva Safety, or related pharmacovigilance systems.

• Ensure compliance with global pharmacovigilance regulations, SOPs, and reporting requirements.

Qualifications

Education

• Bachelor's degree in any of the following:

  • Pharmacy

  • Nursing

  • Medical Technology

  • Medical Laboratory Science

  • Biomedical Science

  • Molecular Biology

  • Pharmaceutical Chemistry

  • Other Life Sciences or Healthcare-related disciplines

Experience

• Strong experience in Pharmacovigilance, Drug Safety, or Case Processing.

• Experience processing and reviewing Individual Case Safety Reports (ICSRs).

• Hands-on experience using Argus Safety, Oracle Argus, Veeva Safety, or similar pharmacovigilance platforms.

• Knowledge of:

  • MedDRA Coding

  • Adverse Event Reporting

  • Safety Narrative Writing

  • ICSR Management

  • Quality Review and Quality Control Processes

Preferred Experience

• Global Pharmacovigilance Operations

• Regulatory Reporting

• WHO Drug Coding

• Clinical Research

• Healthcare BPO Operations

• Life Sciences Shared Services
  

Why Join Us?

• Opportunity to be part of a growing and specialized Pharmacovigilance team

• Exposure to global drug safety and regulatory compliance operations

• Career growth opportunities within Pharmacovigilance, Drug Safety, and Life Sciences

• Collaborative environment with industry experts and healthcare professionals

Make an impact on global patient safety and healthcare outcomes. Apply today and grow your career in Pharmacovigilance with us.