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Pharmacovigilance Services Associate

0-3 years
Not Disclosed
10 Dec. 26, 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
Required Skill: Pharmacovigilance & Drug Safety Surveillance
Location: Accenture
Qualifications: Bachelor of Pharmacy/Bachelor of Physiotherapy/BSc. Nursing
Experience: 0-3 years


About Accenture
Accenture is a global professional services company, known for its leadership in digital, cloud, and security. We deliver unmatched experience and specialized skills across more than 40 industries, offering services in Strategy and Consulting, Technology and Operations, and Accenture Song. Powered by the world's largest network of Advanced Technology and Intelligent Operations centers, Accenture employs 699,000 people serving clients in over 120 countries. Our mission is to embrace the power of change, creating value and shared success for our clients, employees, shareholders, partners, and communities.


Role Overview
As a Pharmacovigilance Services Associate within Accenture's Life Sciences R&D vertical, you will support the company's efforts in improving patient outcomes. Your role will focus on pharmacovigilance services, including case identification, data entry, MedDRA coding, case processing, submission, and follow-up of Individual Case Safety Reports (ICSRs) in compliance with client guidelines and global regulatory requirements. You will be responsible for managing the Affiliate Mailbox, reconciling reports, and handling both serious and non-serious cases.

Key Responsibilities:

  • Manage case identification, data entry, MedDRA coding, and processing of ICSRs in the safety database.
  • Perform written follow-up attempts as per process for serious and non-serious cases.
  • Reconcile reports per process, adhering to client-specific guidelines.
  • Solve routine problems using established guidelines, with limited autonomy.
  • Work within a team, under the direction of a supervisor, to contribute to team objectives.
  • Execute tasks with detailed to moderate instruction, ensuring accuracy and compliance.
  • Potential for working in rotational shifts as required by business needs.

What We’re Looking For:

  • Ability to work well under pressure and adapt quickly to new information.
  • Strong teamwork skills and a collaborative approach.
  • Agility in learning new tasks and processes.
  • A flexible and adaptable mindset to meet evolving client needs.