Accelerated Development Program (Start ASAP)

Northwestern University; Taguig; On-site; PHP 279,000 - 390,600; Full time

Job summary

A leading educational institution is hiring a Pharmacovigilance Associate in Taguig, Philippines. The role involves monitoring drug safety data, collaborating with cross-functional teams, analyzing adverse event reports, and supporting the development of safety protocols. Ideal candidates should have up to 1 year of experience in Pharma Research & Development and possess strong analytical and communication skills. This position offers a hybrid work model with rotational shifts.

Qualifications

• 0 - 1 years of experience in Pharma Research & Development.
• Proficiency in safety data analysis.
• Knowledge of PV Case Processing.
• Familiarity with regulatory requirements.

Responsibilities

• Monitor and assess drug safety data.
• Collaborate with cross-functional teams.
• Analyze adverse event reports.
• Support development of safety protocols.
• Conduct research on safety concerns.

Skills

Pharma Research & Development

Drug safety data analysis

Regulatory compliance

Communication skills

Attention to detail

Adaptability to shifts

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

How to Apply

Applicants may be required to attend interviews in person or by video conference and present current state or government issued ID during each interview.

This job may close before the stated closing date, you are encouraged to apply as soon as possible

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