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Spe-Pharmacovigilance

Cognizant
Cognizant
2-5 years
Not Disclosed
10 Jan. 8, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Specialist – Pharmacovigilance (SPE)

Job ID: 00066161831
Location: Taguig, NC – 1st to 4th Floor, Philippines
Job Category: Digital / Pharmacovigilance
Work Model: Hybrid | Day Shift
Experience Required: 2–5 years in Pharmacovigilance / Safety Operations


Job Summary

Join our innovative team as a Specialist in Pharmacovigilance (SPE), where you will leverage your expertise in Generative AI, Prompt Engineering, and PV Case Processing to enhance drug safety operations. This hybrid role allows flexible on-site and remote work while contributing to research, development, and operational excellence in pharmacovigilance.

You will play a key role in ensuring compliance with global safety regulations, improving efficiency in case processing, and supporting strategic initiatives that enhance patient safety and product quality.


Key Responsibilities

  • Oversee pharmacovigilance case processing to ensure compliance with regulatory requirements and organizational standards.

  • Utilize Generative AI and Prompt Engineering to streamline safety workflows, improve efficiency, and enhance data quality.

  • Collaborate with cross-functional teams to support research and development projects, contributing to innovative safety strategies.

  • Analyze safety data to identify trends, detect potential safety signals, and enhance the overall safety profile of healthcare products.

  • Maintain accurate and timely documentation using MS Office and reporting tools to support regulatory submissions.

  • Participate in continuous learning and professional development in pharmacovigilance and safety operations.

  • Contribute to the development and implementation of best practices, SOPs, and quality improvement initiatives.

  • Provide updates and communicate effectively with internal and external stakeholders regarding safety activities and findings.

  • Assist in preparing regulatory reports and submissions in accordance with global standards.

  • Promote a culture of safety, compliance, and quality throughout the organization.


Required Qualifications

  • Strong experience in PV Case Processing, Pharmacovigilance, and Safety Operations.

  • Proficiency in Generative AI, Prompt Engineering, and MS Office for documentation and reporting.

  • Excellent research and analytical skills to support safety and R&D initiatives.

  • Native or advanced English proficiency with strong verbal and written communication skills.

  • Commitment to continuous learning and professional development in the pharmacovigilance domain.


Preferred Certifications

  • Certification in Pharmacovigilance or related field is highly preferred.


Why Join Cognizant

Cognizant provides a collaborative, high-performance environment where innovation and patient safety are prioritized. Team members benefit from:

  • Exposure to global pharmacovigilance operations and cutting-edge AI applications.

  • Career growth opportunities through training, mentorship, and skill development.

  • An inclusive and supportive workplace culture focused on quality, compliance, and innovation.


Equal Opportunity

Cognizant is an equal opportunity employer, ensuring all qualified candidates receive consideration regardless of race, color, sex, religion, sexual orientation, gender identity, national origin, disability, veteran status, or other legally protected characteristics.