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    Pharmacovigilance Services Analyst

    Accenture
    3-5 years
    Not Disclosed
    Bangalore
    10 Sept. 27, 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 Description

    Position: Pharmacovigilance Services Analyst
    Skill Required: Customer Acquisition Strategy & Implementation
    Qualifications: Any Graduation
    Experience: 3 - 5 Years

    About Accenture

    Accenture is a global professional services company with leading capabilities in digital, cloud, and security. With unmatched experience across over 40 industries, we provide Strategy and Consulting, Technology and Operations services, and Accenture Song—powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our team of 699,000 individuals serves clients in more than 120 countries, leveraging the power of change to create value and shared success for our clients, employees, shareholders, partners, and communities. Learn more at www.accenture.com.

    What You Will Do

    As a Pharmacovigilance Services Analyst, you will be aligned with our Life Sciences R&D vertical. Our services encompass the entire life sciences spectrum, including research laboratories, clinical trial support, regulatory services, pharmacovigilance, and patient services solutions. You will contribute to our Clinical, Pharmacovigilance & Regulatory sub-offering, assisting leading biopharma companies in enhancing patient outcomes by integrating scientific expertise with insights into the patient experience.

    Your responsibilities will include:

    • Supporting public disclosure of clinical documents in accordance with client and regulatory requirements.
    • Redacting clinical documents to protect the privacy of individuals and groups involved in clinical studies for public availability post-approval from EU and US regulatory authorities.
    • Removing or redacting privacy data from clinical documents as per the Redaction Checklist.
    • Conducting quality reviews of redacted clinical documents following specific guidelines.
    • Finalizing fully redacted documents and ensuring tasks, including redaction and incorporation of QC comments, are completed within agreed timelines.
    • Being well-versed in EU Policy 70 and Health Canada guidelines on clinical trial data transparency.
    • Demonstrating thorough knowledge of redaction and anonymization techniques.
    • Preparing anonymization reports and justification tables.

    What We Are Looking For

    • Strong ability to establish client relationships
    • Effective management of multiple stakeholders
    • Capacity to meet deadlines
    • Ability to perform well under pressure

    Roles and Responsibilities

    • Analyze and solve increasingly complex problems.
    • Interact daily with peers within Accenture, with occasional client and management interactions.
    • Receive minimal instruction on daily tasks and moderate guidance on new assignments.
    • Make decisions that impact your own work and may affect the work of others.
    • Operate as an individual contributor and/or oversee a small team or work effort.
    • Note: This role may require working in rotational shifts.

    Join us at Accenture and play a pivotal role in advancing pharmacovigilance and patient safety!

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