Data Management Job at Pfizer | M Pharma Candidates Apply Now

DPharma Jobs at Pfizer | M Pharma Candidates Apply Now  

Looking to launch your pharmaceutical career with a global leader? Pfizer is hiring an Associate Safety Data Management Specialist in Chennai, India. This exciting opportunity allows you to be part of a world-class team focused on ensuring the safe and effective use of medicines. If you have a passion for healthcare, attention to detail, and 1–2 years of relevant experience, this could be your next big career move.

About the Company:

At Pfizer, our Worldwide Medical and Safety colleagues play a vital role in connecting evidence-based medical decision support with stakeholders to improve health and treatment outcomes. Our mission is focused on empowering healthcare decisions related to the safe and effective use of medicines for patients. Pfizer is one of the world’s premier biopharmaceutical companies, committed to discovering, developing, and delivering innovative medicines that improve lives. With a strong focus on science and a global presence, Pfizer works to advance wellness, prevention, treatments, and cures across a broad range of therapeutic areas. The company is driven by its purpose—Breakthroughs that change patients’ lives—and it continues to set industry standards for safety, quality, and integrity. With operations in over 150 countries

, Pfizer offers a dynamic and inclusive workplace where your work can truly make an impact on global health.

Job Details:

Position: Associate – Safety Data Management Specialist

Location: Chennai, India

Employment Type: Full-time

Job Requisition ID: 4939465

Work Location Assignment: Hybrid

Minimum Requirements:

  • Education: B. Pharm, M. Pharm, or D Pharm only
  • Minimum experience: 1 year, Maximum: 2 years
  • Ability to work collaboratively in a team environment

Bonus Points If You Have:

  • Hands-on experience in the ARGUS safety database
  • Proficiency with processing source documents in XML format
  • Good knowledge of medical terminology and global regulatory requirements

Primary Responsibilities:

  • Carry out case processing activities
  • Review, rank, verify, process, and document case-related information
  • Write and edit the case narrative
  • Liaise with key partners for safety data collection

Pfizer is an equal opportunity employer and adheres to all applicable equal employment opportunity laws in every jurisdiction where it operates.

APPLY ONLINE HERE

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