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Pharmacovigilance Services Associate

0-3 years
Not Disclosed
10 Sept. 27, 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 of 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 across more than 40 industries, we provide Strategy and Consulting, Technology and Operations services, and Accenture Song—driven by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our team of 699,000 individuals serves clients in over 120 countries, embracing change to create value and shared success for our clients, people, shareholders, partners, and communities. Learn more at www.accenture.com.


What You Will Do

As a Pharmacovigilance Services Associate, you will be part of our Life Sciences R&D vertical. Our services cover the entire life sciences enterprise, from research laboratories and clinical trial support to regulatory services, pharmacovigilance, and patient services solutions. You will contribute to one of our sub-offerings—Clinical, Pharmacovigilance & Regulatory—helping leading biopharma companies enhance patient outcomes by merging scientific expertise with insights into the patient experience.

Your responsibilities will include managing the Affiliate Mailbox, reconciling reports, and performing all written follow-up attempts for both Serious and Non-serious cases. You will be expected to create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for Individual Case Safety Reports (ICSRs) in compliance with client guidelines and global regulatory requirements.


What We Are Looking For

  • Ability to perform under pressure
  • Strong teamwork skills
  • Adaptability and flexibility
  • Quick learning agility

Roles and Responsibilities

  • Solve routine problems primarily through established guidelines and precedents.
  • Interact primarily with your team and direct supervisor.
  • Receive detailed to moderate instruction for daily tasks and comprehensive guidance for new assignments.
  • Make decisions that impact your individual work.
  • Operate as an individual contributor within a focused team scope.
  • Note: This role may require working in rotational shifts.

Join us at Accenture and contribute to shaping the future of pharmacovigilance and patient safety!