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Jr Pharmacovigilance Analyst

1+ years
Not Disclosed
10 Dec. 5, 2024
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Pharmacovigilance Specialist – Market Research

Location: São Paulo, SP (4 days on-site)

About IQVIA
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at IQVIA Careers.

Job Overview
Responsible for the management and delivery of excellence for assigned projects, focusing on Lifecycle Safety functions, particularly in post-market Pharmacovigilance related to Market Research.

Essential Functions

  • Project Management:

    • Manage customer communication and interface for assigned projects.
    • Represent Lifecycle Safety on Market Research initiatives.
    • Ensure continuity in project design and delivery through strong customer engagement.
  • Pharmacovigilance Support:

    • Oversee Pharmacovigilance deliverables for assigned projects.
    • Provide accountability for local Pharmacovigilance activities, supporting the regional team in processing Adverse Events (AEs) from Market Research.
    • Collaborate with leadership to implement compliance initiatives and ensure global process consistency.
  • Quality Assurance:

    • Manage quality for assigned projects and ensure adherence to Quality Management metrics and policies.
    • Engage with local and global Market Research teams to ensure compliance.
  • Risk Mitigation:

    • Support Market Research and Consulting teams during new project initiation.
    • Identify potential risks from Pharmacovigilance, ESOMAR, and GDPR perspectives, implementing mitigation measures for seamless project delivery.
  • Stakeholder Collaboration:

    • Attend internal and external stakeholder meetings to provide project status updates and define processes.
    • Act as a liaison during client audits and inspections, contributing to Corrective Action Plans in collaboration with Quality Assurance.
  • Additional Duties:

    • Perform other related tasks as assigned.

Qualifications

  • Education:

    • Bachelor’s Degree in Health Sciences or a directly related field.
  • Experience:

    • Minimum 1 year in Lifecycle Safety (Pharmacovigilance, Medical Information, Risk Management, etc.).
    • Knowledge of global, regional, and local Pharmacovigilance regulations.
  • Skills:

    • Effective verbal and written communication skills.
    • Strong organizational and prioritization abilities with attention to critical timelines.
    • Proficiency in Power Query and Excel is a plus.
    • Creative, innovative, and proactive approach to problem-solving.
  • Language:

    • Intermediate English proficiency.

Work Requirements:

  • Availability to work on-site 4 days per week at São Paulo/SP office.

Why IQVIA?
IQVIA values diversity and innovation while fostering a collaborative and inclusive work environment. We offer competitive compensation, opportunities for professional growth, and a strong commitment to improving healthcare outcomes globally.


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