Pharmacovigilance Clinician - Safety & Risk Lead

Wipro Ltd.; Philippines; On-site; PHP 600,000 - 1,200,000; Full time

Job summary

Wipro Limited in Quezon City, Philippines, is seeking a Clinician for Pharmacovigilance to lead medical safety input, risk assessment, and post‑market surveillance activities. The role collaborates with the Medical Safety Officer and cross‑functional teams to ensure robust safety processes and regulatory compliance.

The ideal candidate has 3–5 years in pharmacovigilance or clinical research, strong analytical skills, and familiarity with FDA or regulatory reporting.

Qualifications

• Bachelor’s degree in an allied health field with licenses.
• 3–5 years in clinical research, pharmacovigilance, or related fields.
• 3–5 years in pharma/medical device industry or clinical experience preferred.
• Regulatory affairs or QA or complaint handling experience preferred.
• Understanding of risk assessment principles preferred.
• Experience interacting with FDA or other regulatory agencies preferred.
• Excellent communications and analytical skills.
• Proficiency with Microsoft Office (Excel, PowerPoint, Access).

Responsibilities

• Collaborate with Medical Safety Officer to ensure medical review input for safety reports and surveillance plans.
• Contribute to risk management, post-market surveillance, and regulatory filings.
• Assist in health hazard evaluations and data review for safety signals and escalation.
• Support development teams with clinical input for risk management documents (FMEA, RMS, PSR).
• Guide complaint handling investigations and ensure proper regulatory reporting of events.

Skills

Communication skills

Analytical skills

Regulatory affairs

Pharmacovigilance knowledge

Education

Bachelor's degree in Allied Health

Tools

Microsoft Office

Job description

Wipro Limited in Quezon City, Philippines, is seeking a Clinician for Pharmacovigilance to lead medical safety input, risk assessment, and post‑market surveillance activities. The role collaborates with the Medical Safety Officer and cross‑functional teams to ensure robust safety processes and regulatory compliance.

The ideal candidate has 3–5 years in pharmacovigilance or clinical research, strong analytical skills, and familiarity with FDA or regulatory reporting.