Pharmacovigilance Specialist
Job Description
Key Skills
1 candidate(s) have already applied for this Job. Apply now
Pharmacovigilance Specialist
Location: Taguig, Philippines
Work Setup: Onsite during training; Hybrid after production
Onsite Requirement: 3x onsite per week upon production
Salary: Up to PHP 37,000 maximum package
Start Date: November 3, 2026
Job Summary
We are looking for a Pharmacovigilance Specialist to support pharmacovigilance and drug safety operations, including safety case processing and data management within pharmacovigilance safety databases.
The ideal candidate should have relevant healthcare or pharmacy experience, strong attention to detail, good communication skills, and the ability to work effectively in a structured, process-driven environment.
Qualifications
Pharmacy graduates are required; candidates may apply with or without an active professional license.
Nursing graduates will also be considered.
1–2 years of experience in pharmacovigilance/safety case processing is preferred.
Experience working with pharmacovigilance safety databases such as Veeva Safety or Argus.
Good written and verbal communication skills.
Strong attention to detail and ability to follow defined processes.
Willingness to work fully onsite during training.
Willingness to work hybrid with 3 days onsite per week upon moving to production.
Candidates should be willing to work in Taguig.
Key Responsibilities
Process and manage safety cases in accordance with pharmacovigilance procedures.
Enter, review, and maintain accurate safety case information in pharmacovigilance databases.
Perform data validation and quality checks on safety cases.
Ensure case processing activities comply with established procedures and quality standards.
Identify discrepancies or missing information and coordinate for resolution.
Maintain accurate and complete documentation.
Collaborate with relevant teams to support timely case processing.
Follow pharmacovigilance processes, guidelines, and regulatory requirements.
Meet established quality and productivity targets.
Work Setup
Location: Taguig, Philippines
Training: Fully Onsite
Production: Hybrid – 3 days onsite per week
Start Date: November 3, 2026
Recruitment Process
Validation (Talkpush) → Talkpush Exam → Virtual or Walk-in Interview
Compensation
Salary: Up to PHP 37,000 maximum package
Pre-Screening Questionnaire
Interested candidates are requested to complete the following questionnaire:
What is your highest educational qualification?
Are you a Pharmacy or Nursing graduate?
Do you have an active professional license? If yes, please specify.
How many years of experience do you have in Pharmacovigilance/Safety Case Processing?
Which pharmacovigilance safety databases have you worked with? (e.g., Veeva Safety, Argus)
Are you willing to work fully onsite during training?
Are you willing to work hybrid with 3 days onsite per week in Taguig after moving to production?
Are you comfortable with the PHP 37,000 maximum package?
What is your current/last drawn salary?
What is your notice period/earliest joining date?
Are you available to start on November 3, 2026?
Apply Now
Please complete the pre-screening questionnaire before submitting your application:
Questionnaire Link: https://myglit.com/lateral/cref/1bcbac2e6b
Role
Clinical Research
Timings
Day Shift (Permanent)
Industry
BPO
Work Mode
Work from office
Process
Voice
Functional Area
Medical Professional / Healthcare Practitioner / Technician
Note: Myglit doesn't charge any money from candidates. If you have been asked to pay money to get this job then report to us immediately at support@myglit.com.
Interview Tips
- Giving the VNA round?
- What are the most important skills you acquired as a Soft Skills/VNA trainer?
- How would you handle an irate customer?
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