Pioneering Pharmacovigilance ICSR Specialist

Private Advertiser; Taguig; On-site; PHP 279,000 - 391,000; Full time

Benefits offered by this job

Joining Bonus

Job summary

Private Advertiser is seeking a Pharmacovigilance Case Processing Associate to support the management of Individual Case Safety Reports (ICSRs) and ensure accurate safety data processing and regulatory compliance. This role focuses on Drug Safety, Pharmacovigilance, Case Processing, Argus Safety, Veeva Safety, MedDRA Coding and Narrative Writing.

Responsibilities include ICSR processing, data entry, case book-in, drafting safety narratives, MedDRA coding, quality checks, and ensuring submission

Qualifications

• 1–2 years of experience in Pharmacovigilance, Drug Safety, or ICSR Processing.
• Hands-on experience with Argus Safety, Veeva Safety, Oracle Argus, Safety Database Systems, or other PV platforms.
• Knowledge of: Case Processing, Medical Coding / MedDRA Coding, Narrative Writing, Quality Review, Adverse Event Reporting.
• Strong English communication skills.

Responsibilities

• Process and manage ICSR (Individual Case Safety Reports)
• Perform case intake, data entry, and case book-in activities
• Prepare and update safety case narratives
• Conduct MedDRA and product coding activities
• Perform quality checks and case reviews
• Manage workflow updates, case routing, and case closure
• Support labeling and regulatory compliance activities
• Ensure timely case reconciliation and submission readiness
• Maintain data accuracy within pharmacovigilance safety databases

Skills

Pharmacovigilance

ICSR Processing

Drug Safety

Argus Safety

Veeva Safety

MedDRA Coding

Narrative Writing

Quality Review

English Proficiency

Education

Bachelor's degree in Pharmacy, Nursing, BS Medical Technology / Medical Laboratory Science, Biomedical Science, Molecular Biology or Pharmaceutical Chemistry

Tools

Argus Safety

Veeva Safety

Oracle Argus

Safety Database Systems

Job description

Private Advertiser is seeking a Pharmacovigilance Case Processing Associate to support the management of Individual Case Safety Reports (ICSRs) and ensure accurate safety data processing and regulatory compliance. This role focuses on Drug Safety, Pharmacovigilance, Case Processing, Argus Safety, Veeva Safety, MedDRA Coding and Narrative Writing.

Responsibilities include ICSR processing, data entry, case book-in, drafting safety narratives, MedDRA coding, quality checks, and ensuring submission