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Pharmacovigilance Services Associate

0-1 years
Not Disclosed
10 Nov. 27, 2024
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Position Title: Associate - Pharmacovigilance Services (Pharmacovigilance & Drug Safety Surveillance)

Required Skills: Pharmacovigilance Services

Qualifications:

  • Bachelor of Pharmacy

Experience:

  • 0 to 1 year

Language Proficiency:

  • English: Advanced

About Accenture

Accenture is a global professional services company with leading expertise in digital, cloud, and security solutions. With unmatched experience and specialized skills across more than 40 industries, we provide services in Strategy and Consulting, Technology and Operations, and Accenture Song. These offerings are supported by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our team of 699,000 professionals delivers innovation and value daily, serving clients in over 120 countries. Together, we harness the power of change to drive success for our clients, people, shareholders, partners, and communities. Visit us at www.accenture.com.


Job Role Overview

You will work in Accenture's Life Sciences R&D vertical, supporting services across the life sciences spectrum, including research laboratories, clinical trials, regulatory services, pharmacovigilance, and patient services. Specifically, you will contribute to the Pharmacovigilance & Regulatory sub-offering, helping biopharma leaders improve outcomes by integrating patient-focused insights with scientific expertise.

Key responsibilities include:

  • Managing the Affiliate Mailbox and reconciling reports as per process guidelines.
  • Performing written follow-ups for both serious and non-serious cases.
  • Case identification, data entry, MedDRA coding, and case processing for Individual Case Safety Reports (ICSRs).
  • Ensuring timely submission and follow-ups in compliance with client and global regulatory requirements.

What We Are Looking For

  • Problem-Solving: Ability to address routine issues using standard guidelines and precedents.
  • Team Interaction: Primarily engaging with your team and direct supervisor.
  • Task Execution: Clear instructions provided for all tasks; decision-making is limited to your scope of work and closely monitored.
  • Individual Contributor Role: You will work within a focused team, performing tasks within a predetermined scope.
  • Work Schedule: Flexibility to work in rotational shifts as required.

Roles and Responsibilities

  • Address routine problems by referring to established guidelines.
  • Collaborate with your team and supervisor for task execution.
  • Perform tasks under detailed instructions and close supervision.
  • Operate as an individual contributor with defined responsibilities.
  • Adapt to rotational shift schedules when needed.