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Accenture

0-1 years
Preferred by Comapny
12 Nov. 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: Associate - Pharmacovigilance Services

Skill Required: Pharmacovigilance & Drug Safety Surveillance
Qualifications: Bachelor of Pharmacy
Experience: 0 to 1 year
Language Ability: English - Advanced


About Accenture

Accenture is a global leader in professional services, with expertise in digital, cloud, and security. With 699,000 employees across 120+ countries, Accenture specializes in strategy and consulting, technology and operations services, and Accenture Song. Leveraging cutting-edge technology and innovation, we drive value creation for clients, people, and communities worldwide.

Learn more at www.accenture.com.


Role Overview

As an Associate in Pharmacovigilance Services, you will work within the Life Sciences R&D vertical, focusing on clinical trials, regulatory services, pharmacovigilance, and patient support solutions. This role enables the world’s leading biopharma companies to improve outcomes by combining scientific expertise with patient insights.


Key Responsibilities

  • Case Management:

    • Create, manage, and process Individual Case Safety Reports (ICSRs).
    • Perform data entry, MedDRA coding, case processing, submission, and follow-ups in compliance with global regulatory requirements.
  • Affiliate Mailbox Management:

    • Reconcile reports as per process guidelines.
    • Perform all written follow-up activities for both serious and non-serious cases.
  • Documentation and Reporting:

    • Ensure adherence to client guidelines and global regulatory standards for safety database management.
  • Team Collaboration:

    • Work closely with your supervisor and team to complete tasks.

What We Are Looking For

  • Problem Solving: Ability to solve routine problems using general guidelines and precedents.
  • Team Interaction: Collaborate with team members and report to the direct supervisor.
  • Task Execution: Follow detailed instructions for all assigned tasks.
  • Decision Impact: Focus on individual contributions with supervised decision-making.
  • Flexibility: Ability to work in rotational shifts, as required by the role.

Why Join Accenture?

  • Be a Part of Innovation: Contribute to impactful projects in the biopharma industry.
  • Collaborative Culture: Work in a team-oriented, supportive environment.
  • Global Impact: Help biopharma companies improve lives by advancing medical innovation.

Start your career journey with Accenture, where innovation meets opportunity!