Accelerated Development Program (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

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