Accelerated Development Program (Start ASAP)

Uc Bcf; Taguig; Hybrid; PHP 300,000 - 420,000; Full time

Job summary

A global pharmaceutical company is seeking a Pharmacovigilance Associate to monitor drug safety data and support pharma R&D. In this hybrid role, you'll assess compliance with regulatory standards and collaborate with teams to enhance processes. Ideal candidates will have 0-1 years of experience and knowledge in safety data analysis. Strong communication and attention to detail are essential. Apply soon as the role may close before the stated date.

Qualifications

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

Responsibilities

• Monitor and assess drug safety data for compliance.
• Collaborate with teams to enhance pharmacovigilance processes.
• Analyze adverse event reports for risk management.
• 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

Skills

Pharma Research & Development

Safety data analysis

Communication skills

Attention to detail

Adaptability

Education

0-1 years in Pharma R&D

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

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