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Pharmacovigilance Subject Matter Expert | ₱30K Joining Bonus

Private Advertiser

Taguig City, Metro ManilaPosted 9 hours agoJobStreet

Setup
Hybrid
Type
Full-time
Level
Mid-level
Salary
PHP 80k–120k/mo
Closes
Open

Skills mentioned

Customer ServiceNursingData EntryLegalPharmaceutical
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About the role

Be Our Pioneer Subject Matter Expert for Pharmacovigilance!₱30,000 Joining Bonus*Terms and conditions apply. Do you have what it takes to make a difference in patient safety? We're looking for experienced Pharmacovigilance Case Processing Associates to join our growing team and be among the first SMEs in our Pharmacovigilance practice. If you have hands-on experience in Drug Safety, ICSR Processing, Argus Safety, Veeva Safety, MedDRA Coding, and Narrative Writing, this is your opportunity to take your career to the next level. Join a team where your expertise helps ensure accurate safety reporting, regulatory compliance, and ultimately contributes to improving patient outcomes worldwide.

What You'll Do

  • Process and manage Individual Case Safety Reports (ICSRs)
  • Perform case intake, data entry, and case book-in activities
  • Prepare and update safety case narratives
  • Utilize MedDRA and product coding
  • Perform quality reviews and case assessments
  • Manage workflow updates, case routing, and case closure
  • Support labeling and regulatory compliance activities
  • Ensure timely reconciliation and submission readiness
  • Maintain data accuracy within pharmacovigilance safety databases
  • Do You Have What It Takes? Education
  • Bachelor's Degree in Pharmacy, Nursing, Medical Technology/Medical Laboratory Science, Biomedical Science, Molecular Biology, or Pharmaceutical Chemistry
  • Professional license is an advantage but not required

Experience

  • 1-2 years of experience in Pharmacovigilance, Drug Safety, or ICSR Processing
  • Experience with Argus Safety, Veeva Safety, Oracle Argus, Safety Database Systems, or other PV platforms
  • Knowledge of: Case Processing

MedDRANarrative Writing

Quality Review

Adverse Event Reporting

  • Strong English communication skills

Preferred Skills✔ ICSR Management✔ MedDRA Utilization✔ WHO Drug Coding✔ Regulatory Reporting✔ Global Pharmacovigilance Operations✔ Clinical Research✔ Drug Safety Surveillance✔ Life Sciences Shared Services or Healthcare BPO experience

  • Why Join Us? Be part of a pioneering team
  • Work with global pharmacovigilance operations
  • Grow your expertise in Drug Safety and Regulatory Compliance

Enjoy a ₱30,000 Joining Bonus*Think you're the right fit? Apply today and bring your Pharmacovigilance expertise to a team where your impact matters.

Sourced from JobStreet · posted 9 hours ago · you apply on the original site