Associate – Safety Data Management Specialist

1 day ago

Chennai, India Pfizer Full time

This job is with Pfizer, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.Use Your Power for PurposeAt Pfizer, our Worldwide Medical and Safety colleagues are pivotal in bridging evidence-based medical decision support with stakeholders to enhance health and treatment outcomes. Whether you are developing frameworks to ensure our evidence is scientifically robust, offering unbiased and medically essential expertise, or exploring ways to address data gaps, our mission remains clear: to empower healthcare decisions regarding the safe and appropriate use of medicines for patients.Primary ResponsibilitiesCarry out case processing activitiesReview, rank, verify, process and document case-related information: event terms; validity, seriousness, special scenarios; timelines; accuracy and consistency.  Process cases based on these assessmentsReview case criteria to determine appropriate workflow for case processingAssess cases to distinguish those with particular complexities and/or specific issues, and escalate appropriatelyWrite and edit case narrativeDetermine and perform appropriate case follow-up, including generation of follow-up requestsReview processed cases to verify accuracy, consistency and compliance with process requirements, and review case data for special scenariosLiaise with key partners, locally, and other stakeholders regarding safety data collection and data reconciliationDevelop 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 databaseDetermine reportability of scheduled reports, ensuring adherence to regulatory requirementsConsistently apply regulatory requirements and Pfizer policiesParticipate, as appropriate, in local, internal and external safety activitiesHere Is What You Need (Minimum Requirements):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.Bonus Points If You Have (Preferred 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.Work Location Assignment: HybridWork Location Assignment: HybridPfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.Medical

  • Associate – Safety Data Management Specialist

    1 day ago

    Chennai, India Pfizer Full time

    Use Your Power for Purpose At Pfizer, our Worldwide Medical and Safety colleagues are pivotal in bridging evidence-based medical decision support with stakeholders to enhance health and treatment outcomes. Whether you are developing frameworks to ensure our evidence is scientifically robust, offering unbiased and medically essential expertise, or exploring...

  • Associate – Safety Data Management Specialist

    3 days ago

    Chennai, Tamil Nadu, India Pfizer Full time ₹ 4,32,000 - ₹ 6,48,000 per year

    Use Your Power for PurposeAt Pfizer, our Worldwide Medical and Safety colleagues are pivotal in bridging evidence-based medical decision support with stakeholders to enhance health and treatment outcomes. Whether you are developing frameworks to ensure our evidence is scientifically robust, offering unbiased and medically essential expertise, or exploring...

  • Associate Safety Data Management Specialist

    1 day ago

    Chennai, India Pfizer Full time

    In this pharmacovigilance role, you will carry out processing activities of Individual Case Safety Reports (both clinical trials and post-marketing sources) in the ARGUS Safety database. Processing activities include assessing case validity, undertaking duplicate checks, creating cases in the database, prioritizing cases as per company guidance, updating...

  • Associate Safety Data Management Specialist

    3 days ago

    Chennai, Tamil Nadu, India Pfizer Full time ₹ 4,00,000 - ₹ 8,00,000 per year

    In this pharmacovigilance role, you will carry out processing activities of Individual Case Safety Reports (both clinical trials and post-marketing sources) in the ARGUS Safety database.Processing activities include assessing case validity, undertaking duplicate checks, creating cases in the database, prioritizing cases as per company guidance, updating...

  • Associate Safety Data Management Specialist

    20 hours ago

    Chennai, Tamil Nadu, India Pfizer Full time ₹ 5,00,000 - ₹ 15,00,000 per year

    In this pharmacovigilance role, you will carry out processing activities of Individual Case Safety Reports (both clinical trials and post-marketing sources) in the ARGUS Safety database.Processing activities include assessing case validity, undertaking duplicate checks, creating cases in the database, prioritizing cases as per company guidance, updating...

  • Associate Safety Data Management Specialist

    2 days ago

    chennai, India Pfizer Full time

    In this pharmacovigilance role, you will carry out processing activities of Individual Case Safety Reports (both clinical trials and post-marketing sources) in the ARGUS Safety database.Processing activities include assessing case validity, undertaking duplicate checks, creating cases in the database, prioritizing cases as per company guidance, updating...

  • Safety Officer

    5 days ago

    Chennai, Tamil Nadu, India Data Patterns Full time

    Designation - Safety Officer - Job Description **Qualification**: ME - Industrial Safety Engineering with 7-9 years of experience in safety Prescribed under Tamil Nadu Factories (Safety officer ) rules 2005 **Skill Set**: Overall responsibility to ensure Health & Safety of operations. Responsible for ensuring compliance with legislative requirements and...

  • Associate Safety Data Management Specialist

    1 day ago

    Chennai, India Pfizer Full time

    This job is with Pfizer, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.In this pharmacovigilance role, you will carry out processing activities of Individual Case Safety Reports (both clinical trials and post-marketing sources) in the ARGUS Safety...

  • Associate Safety Data Management Specialist

    2 weeks ago

    Chennai, India myGwork - LGBTQ+ Business Community Full time

    Job Description This job is with Pfizer, an inclusive employer and a member of myGwork the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. In this pharmacovigilance role, you will carry out processing activities of Individual Case Safety Reports (both clinical trials and post-marketing sources) in the...

  • Specialist - Environmental Health and Safety

    2 weeks ago

    Chennai, India NTT Full time

    JOB DESCRIPTION Make an impact with NTT DATA Join a company that is pushing the boundaries of what is possible. We are renowned for our technical excellence and leading innovations, and for making a difference to our clients and society. Our workplace embraces diversity and inclusion – it’s a place where you can grow, belong and thrive. Your day at NTT...