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    Pharmacovigilance Services Associate

    Accenture
    0-3 years
    Not Disclosed
    Chennai
    10 Oct. 30, 2024
    Job Description
    Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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 Associate
    Skill Required: Pharmacovigilance & Drug Safety Surveillance
    Qualifications: Bachelor of Pharmacy / Bachelor in Physiotherapy / BSc. Nursing
    Experience: 0 to 3 years

    About Accenture:
    Accenture is a global professional services company with leading capabilities in digital, cloud, and security. Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song—all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in over 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners, and communities. Visit us at www.accenture.com.

    What You Will Do:
    You will be aligned with our Life Sciences R&D vertical, participating in services that span the entire life sciences enterprise, including research laboratories, clinical trials support, regulatory services, and pharmacovigilance. As part of the Clinical, Pharmacovigilance & Regulatory team, your responsibilities will include:

    • Managing the Affiliate Mailbox and reconciling reports.
    • Performing written follow-ups for both serious and non-serious cases.
    • Creating and managing case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for Individual Case Safety Reports (ICSRs) in the safety database in accordance with client guidelines and global regulatory requirements.

    What We’re Looking For:
    Candidates should possess:

    • Adaptability and flexibility.
    • Quick learning agility.
    • A commitment to quality.
    • The ability to perform under pressure.

    Roles and Responsibilities:

    • Solve routine problems largely through precedent and referral to general guidelines.
    • Interact primarily within your own team and with your direct supervisor.
    • Receive detailed to moderate instructions on daily tasks and comprehensive guidance on new assignments.
    • Make decisions that impact your own work.
    • Work as an individual contributor within a team, focused on a predetermined scope of work.

    Please Note: This role may require you to work in rotational shifts.

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