Join Pfizer as a Safety Data Management Specialist Associate- Apply before 25th April, 2024

  • Full Time
  • Chennai

Website Pfizer

About Pfizer

Pfizer is one of the world’s largest pharmaceutical companies, with a long history dating back to its founding in 1849. Headquartered in New York City, Pfizer has established itself as a key player in the global healthcare industry. The company is renowned for its research, development, manufacturing, and distribution of a wide range of prescription medicines, vaccines, and consumer healthcare products.

Pfizer’s portfolio covers various therapeutic areas, including cardiovascular diseases, oncology, neuroscience, immunology, rare diseases, and vaccines. Some of its well-known products include Viagra (sildenafil) for erectile dysfunction, Lipitor (atorvastatin) for high cholesterol, and Prevnar 13 (pneumococcal 13-valent conjugate vaccine) for pneumococcal disease.

In addition to its focus on human health, Pfizer also has a presence in animal health, providing medications and vaccines for livestock and companion animals.

Over the years, Pfizer has been at the forefront of pharmaceutical innovation, investing heavily in research and development to address unmet medical needs and improve patient outcomes. The company has a global presence, with operations in numerous countries and a diverse workforce dedicated to advancing healthcare worldwide.

Pfizer has also been involved in several high-profile partnerships and acquisitions, further expanding its reach and capabilities in the healthcare sector. Notably, Pfizer has played a pivotal role in the development of COVID-19 vaccines, including the widely used mRNA vaccine developed in collaboration with BioNTech.

Associate – Safety Data Management Specialist

Job Description

  • Case Processing: Execute case processing activities ensuring accuracy and consistency.
  • Information Review: Review, verify, and document case-related information including event terms, validity, seriousness, and timelines.
  • Workflow Management: Determine appropriate workflow for case processing based on case criteria.
  • Complex Case Assessment: Identify and escalate cases with complexities or specific issues for appropriate action.
  • Case Narrative: Write and edit case narratives to accurately represent case details.
  • Follow-up: Perform case follow-up activities and generate follow-up requests as necessary.
  • Quality Assurance: Review processed cases to ensure accuracy, consistency, and compliance with process requirements.
  • Stakeholder Liaison: Collaborate with key partners and stakeholders on safety data collection and reconciliation.

Candidate Profile

  • Education: B.Pharm./ M.Pharm./ Pharm D graduates with 2-3 years of experience in ICSR case processing.
  • Attention to Detail: Demonstrate meticulous attention to detail and accuracy in work.
  • Communication Skills: Possess good written communication skills.
  • Analytical Skills: Exhibit analytical and problem-solving skills.
  • Medical Terminology: Proficient in medical terminology.
  • Regulatory Knowledge: Familiarity with ICSR processing guidelines, regulations, and event assessment.
  • Database Experience: Working experience in ARGUS database.

Additional Information

  • Qualification: B.Pharm./ M.Pharm./ Pharm.D
  • Experience: 2-3 years
  • Location: Chennai
  • Industry Type: Pharma
  • End Date: 25th April 2024

This position requires candidates with a strong pharmaceutical background, attention to detail, and proficiency in safety data management processes. If you meet the qualifications and are eager to contribute to Pfizer’s commitment to healthcare, we encourage you to apply before the deadline.

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