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    Pharmacovigilance Services Associate

    Accenture
    1-3 years
    Not Disclosed
    Chennai
    10 Oct. 25, 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 Operations - Drug Safety Surveillance
    Qualifications: Any Graduation
    Experience: 1 - 3 Years

    About Accenture

    Accenture is a global professional services company with leading capabilities in digital, cloud, and security. With unmatched experience across more than 40 industries, we provide 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 change to create value and shared success for our clients, employees, shareholders, partners, and communities. Visit us at www.accenture.com.

    What Will You Do?

    You will be aligned with our Life Sciences R&D vertical, contributing to services that span the entire life sciences enterprise—from research laboratories and clinical trials support to regulatory services and pharmacovigilance. As a Pharmacovigilance Services Associate, you will help leading biopharma companies improve outcomes by connecting scientific expertise with insights into the patient experience.

    Key Responsibilities

    • Manage the Affiliate Mailbox and reconcile reports according to process.
    • Perform all written follow-up attempts for both Serious and Non-serious cases.
    • Create and manage case identification, data entry, MedDRA coding, case processing, and submission for ICSRs in the safety database per client guidelines and applicable global regulatory requirements.
    • Conduct analysis and solve lower-complexity problems.
    • Interact daily with peers within Accenture and provide updates to supervisors.
    • Follow moderate level instructions on daily tasks and detailed instructions on new assignments.
    • Make decisions that impact your own work and may affect others.
    • Work as an individual contributor within a team, focusing on specific tasks.
    • Be prepared to work in rotational shifts as required.

    What Are We Looking For?

    • Strong organizational skills and attention to detail.
    • Ability to analyze and resolve problems effectively.
    • Effective communication skills for interaction with team members and management.
    • Flexibility to adapt to changing tasks and priorities.

    Join Accenture and be a part of a team dedicated to making a meaningful impact in the field of pharmacovigilance and drug safety surveillance.

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