Accelerated Development Program

ByteDance Philippines; Taguig; Hybrid; PHP 279,000 - 502,000; Full time

Job summary

Cognizant Philippines is seeking a Pharmacovigilance Associate to monitor drug safety data and support pharma R&D in a hybrid, rotational shift role.

You will review safety reports, collaborate with cross-functional teams, and help develop safety protocols while ensuring regulatory compliance. Ideal candidates have 0–1 year in Pharma R&D, strong attention to detail, and good communication.

Qualifications

• 0–1 year of experience in Pharma Research & Development.
• Proficiency in safety data analysis.
• Knowledge of PV Case Processing and its impact on drug safety.
• Familiarity with pharmacovigilance regulatory requirements.
• Excellent communication and collaboration skills.

Responsibilities

• Monitor and assess drug safety data to ensure regulatory compliance.
• Collaborate with cross-functional teams to enhance pharmacovigilance processes.
• Analyze adverse event reports and provide insights for risk management.
• Support safety protocol development for pharmaceutical products.
• Prepare safety reports for regulatory submissions.
• Assist in training and continuous improvement of PV systems.

Skills

Pharma R&D

Safety data analysis

Regulatory awareness

Tools

PV Case Processing

Job description

Join Cognizant as a Pharmacovigilance Associate to monitor drug safety data and support pharma R&D in a hybrid, rotational shift role.

Your Role

Key responsibilities include:

• Monitor and assess drug safety data to ensure compliance with regulatory standards
• Collaborate with cross-functional teams to enhance pharmacovigilance processes
• Analyze adverse event reports and provide insights for risk management strategies
• Support the development of safety protocols and guidelines for pharmaceutical products
• Conduct thorough research to identify potential safety concerns and recommend solutions
• Assist in the preparation of safety reports for submission to regulatory authorities
• Utilize Pharma Research & Development skills to improve case processing efficiency
• Participate in training sessions to stay updated on industry best practices
• Contribute to the continuous improvement of pharmacovigilance systems and methodologies
• Ensure accurate documentation of all safety-related activities and findings
• Facilitate communication between stakeholders to address safety issues promptly
• Implement strategies to enhance the quality and reliability of safety data
• Provide technical support in the analysis and interpretation of complex safety data

About You

The company is looking for:

• 0 - 1 years of experience in Pharma Research & Development
• Proficiency in Pharma Research & Development with a focus on safety data analysis
• Knowledge of PV Case Processing and its impact on drug safety
• Familiarity with regulatory requirements related to pharmacovigilance
• Excellent communication skills to collaborate with diverse teams
• Attention to detail in documenting safety-related activities
• Adaptability to rotational shifts and hybrid work model
• Eagerness to learn and stay updated on pharmacovigilance trends