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    Pharmacovigilance Services New Associate

    Accenture
    0-1 years
    Not Disclosed
    Bangalore
    10 Aug. 14, 2024
    Job Description
    Job Type: Full Time Education: B.Sc. 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 Services New Associate

    Skill Required: Pharmacovigilance & Drug Safety Surveillance

    Qualification: BSc

    Experience: 0 to 1 year

    Language Proficiency: English - Proficient

    About Accenture:

    Accenture is a global professional services company with leading capabilities in digital, cloud, and security. We leverage unmatched experience and specialized skills across more than 40 industries, offering Strategy and Consulting, Technology and Operations services, and Accenture Song. With 699,000 employees across more than 120 countries, we are dedicated to delivering the promise of technology and human ingenuity to create value and shared success. Learn more at www.accenture.com.

    Role Overview:

    As a Pharmacovigilance Services New Associate, you will join our Life Sciences R&D vertical, focusing on pharmacovigilance and drug safety surveillance. You will be involved in various activities related to case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for Individual Case Safety Reports (ICSRs). This role is critical to ensuring compliance with client guidelines and global regulatory requirements.

    Key Responsibilities:

    • Case Management: Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database.
    • Data Handling: Reconcile reports as per processes and manage the Affiliate Mailbox.
    • Compliance: Ensure adherence to client guidelines and global regulatory requirements.
    • Documentation: Perform all written follow-up attempts for both serious and non-serious cases.

    Qualifications and Skills:

    • Education: Bachelor’s degree in Life Sciences or related field.
    • Experience: 0 to 1 year in pharmacovigilance or a related field.
    • Skills:
      • Adaptability and flexibility.
      • Ability to perform under pressure and work well in a team.
      • Commitment to quality.
      • Strong written and verbal communication.
      • Knowledge of pharmacovigilance & drug safety surveillance and clinical data management.

    Working Conditions:

    • Team Interaction: Primary interaction within your own team and with your direct supervisor.
    • Decision-Making: Follow detailed instructions with closely supervised decision-making.
    • Work Scope: Individual contributor role with a narrow, predetermined scope of work.
    • Shifts: May require working in rotational shifts.

    If you are committed to quality and have a passion for improving patient outcomes through drug safety, we encourage you to apply and be part of our dynamic team at Accenture.

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