Pharmacovigilance Specialist - Onsite Training, Hybrid

Gratitude Philippines; Manila; Hybrid; PHP 312,000 - 413,000; Full time

Job summary

Gratitude Philippines is seeking a Pharmacovigilance Specialist in Taguig. Onsite training is required, with a hybrid work setup after production. Ideal candidates have pharmacy or nursing backgrounds and 1–2 years in pharmacovigilance, plus experience with Veeva Safety or Argus.

The role focuses on safety case processing, data management, and adherence to pharmacovigilance procedures in a structured environment with clear quality standards.

Qualifications

• Pharmacy graduates are required.
• Nursing graduates will also be considered.
• 1–2 years of experience in pharmacovigilance/safety case processing preferred.
• Experience 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 production.

Responsibilities

• Process and manage safety cases in accordance with pharmacovigilance procedures.
• Enter, review, and maintain safety case information in pharmacovigilance databases.
• Perform data validation and quality checks on safety cases.
• Ensure case processing activities comply with procedures and quality standards.
• Identify discrepancies or missing information and coordinate resolution.
• Maintain accurate and complete documentation.
• Collaborate with relevant teams to support timely case processing.
• Follow pharmacovigilance processes, guidelines, and regulatory requirements.

Skills

Attention to detail

Good communication

Education

Pharmacy graduates

Nursing graduates

Tools

Veeva Safety

Argus

Job description

Gratitude Philippines is seeking a Pharmacovigilance Specialist in Taguig. Onsite training is required, with a hybrid work setup after production. Ideal candidates have pharmacy or nursing backgrounds and 1–2 years in pharmacovigilance, plus experience with Veeva Safety or Argus.

The role focuses on safety case processing, data management, and adherence to pharmacovigilance procedures in a structured environment with clear quality standards.