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Pharmacovigilance Services Associate

1-3 years
Not Disclosed
10 Oct. 9, 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 Associate
Skill Required: Pharmacovigilance & Drug Safety Surveillance
Qualifications: Bachelor of Pharmacy
Experience: 1 to 3 years
Language Proficiency: Advanced English


About Accenture

Accenture is a global professional services company with leading capabilities in digital, cloud, and security. With 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 team of 699,000 people delivers on the promise of technology and human ingenuity every day, serving clients in over 120 countries. We embrace change to create value and shared success for our clients, people, shareholders, partners, and communities. Visit us at www.accenture.com.


What You Will Do

As a Pharmacovigilance Services Associate, you will be aligned with our Life Sciences R&D vertical. Your role will span the entire life sciences enterprise, from research laboratories and clinical trials support to regulatory services, pharmacovigilance, and patient services solutions. You will help leading biopharma companies improve outcomes by connecting scientific expertise with insights into the patient experience.

Key responsibilities include:

  • Managing the Affiliate Mailbox and reconciling reports per process.
  • Performing written follow-up attempts for both Serious and Non-serious cases.
  • Creating and managing case identification, data entry, MedDRA coding, case processing, submissions, and follow-ups for Individual Case Safety Reports (ICSRs) in the safety database according to client guidelines and global regulatory requirements.

What We Are Looking For

In this role, you will be expected to solve routine problems primarily using established guidelines and precedents. Your interactions will mainly be within your team and with your direct supervisor.

Key Responsibilities:

  • Follow detailed to moderate instructions for daily tasks and receive comprehensive guidance for new assignments.
  • Make decisions that will impact your own work within a predetermined, focused scope.
  • Work as an individual contributor within a team environment.
  • Be prepared to work in rotational shifts as required.

If you are ready to contribute to our mission of improving patient outcomes, we invite you to apply!