Accelerated Development Program (Start ASAP)

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

Job summary

A leading educational institution in Taguig is seeking a Pharmacovigilance Associate to monitor drug safety data and support pharmaceutical R&D. Key responsibilities include assessing compliance with regulatory standards, collaborating with teams, and analyzing adverse event reports. Ideal candidates will have a basic understanding of Pharma R&D, a keen eye for detail, and excellent communication skills. This is a hybrid, rotational shift role offering opportunities for growth in the pharmacovigilance field.

Qualifications

• 0 - 1 years of experience in Pharma Research & Development.
• Knowledge of PV Case Processing and its impact on drug safety.
• Familiarity with regulatory requirements related to pharmacovigilance.

Responsibilities

• Monitor and assess drug safety data.
• Collaborate with cross-functional teams.
• Analyze adverse event reports.

Skills

Proficiency in Pharma Research & Development

Excellent communication skills

Attention to detail

Adaptability to rotational 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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