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Pharmacovigilance Services Associate

0-3 years
Not Disclosed
10 Sept. 23, 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, Bachelor in Physiotherapy, or BSc in Nursing
Experience: 0 to 3 years


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. Our team of 699,000 professionals delivers on the promise of technology and human ingenuity, serving clients in over 120 countries. We embrace change to create value and shared success for our clients, employees, shareholders, partners, and communities. Visit us at www.accenture.com.


Role Overview

As a Pharmacovigilance Services Associate, you will be part of our Life Sciences R&D vertical, contributing to the entire life sciences enterprise. Our services include research laboratories, clinical trial support, regulatory services, pharmacovigilance, and patient solutions. You will play a vital role in helping leading biopharma companies improve outcomes by integrating scientific expertise with patient insights.


Key Responsibilities

  • Case Management:
    Handle the management of the Affiliate Mailbox, reconciliation of reports, and performance of follow-ups for both Serious and Non-serious cases.

  • Data Processing:
    Create and manage case identification, data entry, MedDRA coding, and submission of Individual Case Safety Reports (ICSRs) in the safety database, adhering to client guidelines and global regulatory requirements.

  • Routine Problem Solving:
    Solve routine problems primarily through established precedents and general guidelines.

  • Collaboration:
    Interact mainly within your team and with your direct supervisor, following detailed instructions for daily tasks and new assignments.

  • Impact of Decisions:
    Make decisions that primarily impact your own work as an individual contributor within a focused team environment.

  • Shift Work:
    Be prepared to work in rotational shifts as required.


What We Are Looking For

  • Adaptability:
    Flexible and able to adjust to changing circumstances.

  • Agility:
    Quick learner with the ability to grasp new concepts swiftly.

  • Commitment to Quality:
    Strong dedication to maintaining high-quality standards.

  • Performance Under Pressure:
    Ability to perform effectively in high-pressure situations.


If you are ready to contribute to patient safety and support the pharmaceutical industry, we encourage you to apply!