Pharmacovigilance Associate - Hybrid Rotation, Start ASAP

Centro Escolar University; Philippines; Hybrid; PHP 240,000 - 420,000; Full time

Job summary

Cognizant is seeking a Pharmacovigilance Associate in a hybrid, rotational shift role to monitor drug safety data and support pharma R&D. You will coordinate with cross-functional teams to enhance pharmacovigilance processes and contribute to risk management strategies.

Responsibilities include analyzing adverse event reports and supporting safety reports for regulatory submissions. The role emphasizes attention to detail, regulatory knowledge, and proactive communication.

Qualifications

• 0–1 years of experience in Pharma R&D.
• Proficiency in safety data analysis and PV case processing.
• Knowledge of regulatory requirements related to pharmacovigilance.
• Excellent communication skills with cross-functional teams.

Responsibilities

• Monitor and assess drug safety data to ensure regulatory compliance.
• Collaborate with cross-functional teams to improve pharmacovigilance processes.
• Analyze adverse event reports and contribute to risk management strategies.
• Assist in preparing safety reports for regulatory submissions.
• Support development of safety protocols and guidelines for pharma products.

Skills

Pharma R&D

Safety data analysis

PV Case Processing

Regulatory knowledge

Communication

Job description

Cognizant is seeking a Pharmacovigilance Associate in a hybrid, rotational shift role to monitor drug safety data and support pharma R&D. You will coordinate with cross-functional teams to enhance pharmacovigilance processes and contribute to risk management strategies.

Responsibilities include analyzing adverse event reports and supporting safety reports for regulatory submissions. The role emphasizes attention to detail, regulatory knowledge, and proactive communication.