BPharm Job at Pfizer | Apply Now for the Safety Data Management Specialist Role
Join Pfizer, a global leader in healthcare innovation, as an Associate – Safety Data Management Specialist in Chennai, India. This BPharm Job offers a unique opportunity to ensure the safety and integrity of medicines through high-quality case processing and data management. This Pfizer Job is ideal for B.Pharm, M.Pharm, or Pharm.D professionals with 1–2 years of experience in pharmacovigilance, this role allows you to make an impact in global drug safety and patient care.
- Job Post: Associate – Safety Data Management Specialist
- Location: Chennai, India
- Job ID: 4943906
About the company
Pfizer is one of the world’s leading biopharmaceutical companies, committed to discovering, developing, and delivering innovative medicines and vaccines that improve lives globally. Headquartered in New York, Pfizer operates in over 125 countries, addressing some of the most challenging healthcare needs in areas such as oncology, immunology, cardiology, and infectious diseases. With a strong focus on scientific excellence, research innovation, and patient-centric healthcare solutions, Pfizer continues to set new benchmarks in advancing global health and well-being, making it a top choice for BPharm graduates seeking jobs.
Primary Responsibilities of the BPharm Job
- Carry out case processing activities
- Review, rank, verify, process and document case-related information: event terms; validity, seriousness, special scenarios; timelines; accuracy and consistency. Process cases based on these assessments
- Review case criteria to determine appropriate workflow for case processing
- Assess cases to distinguish those with particular complexities and/or specific issues, and escalate appropriately
- Write and edit case narrative
- Determine and perform appropriate case follow-up, including generation of follow-up requests
- Review processed cases to verify accuracy, consistency and compliance with process requirements, and review case data for special scenarios
- Liaise with key partners, locally, and other stakeholders regarding safety data collection and data reconciliation
- Develop and maintain expertise and knowledge for applicable corporate and global regulations, for guidelines, Standard Operating Procedures, for data entry conventions, and for search functions in the safety database
- Determine reportability of scheduled reports, ensuring adherence to regulatory requirements
- Consistently apply regulatory requirements and Pfizer policies
- Participate, as appropriate, in local, internal and external safety activities
Education and Experience
- Education – B. Pharm, M. Pharm, or Pharm. D only.
- Minimum experience – 1 year. Maximum – 2 years.
- Knowledge of ICSR processing.
- Ability to work collaboratively in a team environment.
Additional Requirements:
- Hands on experience in ARGUS safety database.
- Proficiency with processing source documents in XML format (E2B R2 and R3).
- Good knowledge of medical terminology and global regulatory requirements for drug safety.
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Securing a BPharm job at Pfizer assures equal treatment.
