Accelerated Development Program (Start ASAP)

Upcap; Taguig; On-site; PHP 223,200 - 334,800; Full time

Job summary

A pharmaceutical company in Metro Manila is seeking a Pharmacovigilance Associate to ensure compliance in drug safety data analysis and support R&D. The ideal candidate should have up to one year of experience in Pharma R&D and be adept at communicating with cross-functional teams. This hybrid role involves monitoring safety data and developing protocols, with an emphasis on detail and safety documentation. Candidates should be adaptable to rotational shifts.

Qualifications

• 0 - 1 years of experience in Pharma Research & Development.
• Proficiency in safety data analysis.
• Knowledge of PV Case Processing and drug safety compliance.
• Familiarity with regulatory requirements for pharmacovigilance.
• Excellent communication skills for team collaboration.

Responsibilities

• Monitor and assess drug safety data for compliance.
• Collaborate with teams to enhance pharmacovigilance processes.
• Analyze adverse event reports for risk management.
• Support safety protocol development for pharmaceuticals.
• Ensure accurate documentation of safety activities.

Skills

Pharma Research & Development

Safety data analysis

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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