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    Pharmacovigilance Services Associate

    Accenture
    1-3 years
    Not Disclosed
    Bangalore
    10 June 3, 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, ICD-10 CM, CPT, HCPCS Coding, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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    Job Opportunity: Pharmacovigilance Services Associate at Accenture

    Skill Required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance
    Designation: Pharmacovigilance Services Associate
    Qualifications: Bachelor of Pharmacy
    Experience: 1 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 more than 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.

    Job Description

    What Would You Do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, including research laboratories, clinical trials support, regulatory services, pharmacovigilance, and patient services solutions. Employees in this area will be part of one of the sub-offerings: Clinical, Pharmacovigilance & Regulatory, helping the world’s leading biopharma companies bring their vision to life by improving outcomes through a patient-centric approach, connecting scientific expertise with unique insights into the patient experience.

    Key Responsibilities:

    • Manage the Affiliate Mailbox and reconcile reports as per 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, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements.

    Desired Skills:

    • Adaptable and flexible
    • Ability to perform under pressure
    • Problem-solving skills
    • Detail orientation

    Roles and Responsibilities:

    • Solve routine problems largely through precedent and referral to general guidelines.
    • Expected interactions are within your own team and direct supervisor.
    • Receive detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments.
    • Make decisions that impact your own work.
    • Serve as an individual contributor as part of a team, with a predetermined, focused scope of work.
    • Please note that this role may require you to work in rotational shifts.

    For more information and to apply, please visit our Careers Page.

    Join Accenture and be part of a team that is making a global impact by enabling leading biopharma companies to improve patient outcomes through innovative pharmacovigilance services.

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