Career in Pharmacovigilance: Pfizer is Hiring Freshers for the Associate Safety Data Management Specialist role in Chennai – Apply Now
Looking to launch your career in Pharmacovigilance? Pfizer is hiring freshers for the Associate Safety Data Management Specialist role in Chennai! This exciting opportunity allows pharmacy graduates (B.Pharm, M.Pharm, or Pharm.D) to gain hands-on experience in safety data processing, case assessment, and global regulatory compliance using the ARGUS Safety database. If you’re detail-oriented, analytical, and eager to grow in the pharmaceutical industry, this could be your perfect career start.
Job Details:
- Job Title: Associate Safety Data Management Specialist
- Location: Chennai
- Mode: Hybrid
About the Company:
Pfizer is one of the world’s leading biopharmaceutical companies dedicated to discovering, developing, and delivering innovative medicines that improve patient lives globally. With a strong focus on research, development, and safety, Pfizer plays a crucial role in ensuring the effectiveness and reliability of therapeutic solutions across diverse medical areas. The company fosters a culture of continuous learning, collaboration, and inclusion, empowering employees to contribute to global healthcare advancements. Working at Pfizer means joining a purpose-driven organization committed to making breakthroughs that change patients’ lives.
Education:
B.Pharm, M.Pharm, or Pharm.D only.
Experience:
Freshers only.
Key Responsibilities:
- Assessing case validity and performing duplicate checks.
- Creating cases in the database and prioritizing them as per company guidelines.
- Updating cases with information provided in XML source documents.
- Identifying adverse events, confirming seriousness, coding products, and performing causality and listedness assessments.
- Drafting case narratives and determining appropriate follow-up.
- Reviewing processed cases for technical accuracy, compliance, and completeness.
Minimum Requirements:
- Strong attention to detail and solid analytical skills.
- Excellent written and oral communication abilities.
- Good collaboration and continuous learning mindset.
Preferred Requirements:
- Certification or training in Pharmacovigilance.
- Knowledge of medical terminology and global drug safety regulations.
- Publications in peer-reviewed journals.
