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Pharmacovigilance Services Specialist

5-10 years
Not Disclosed
10 Sept. 16, 2025
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 Specialist
Skill Required: Pharmacovigilance Services – Pharmacovigilance & Drug Safety Surveillance
Qualification: MBBS
Experience: 7–11 years
Location: [Not specified in original, can be added if known]
Organization: Accenture


About Accenture

Accenture is a global professional services company with leading capabilities in digital, cloud, and security. Combining unmatched experience and specialized skills across more than 40 industries, we offer:

  • Strategy & Consulting

  • Technology & Operations services

  • Accenture Song

All powered by the world’s largest network of Advanced Technology and Intelligent Operations centers.

Our 699,000 people deliver the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for clients, people, shareholders, partners, and communities.
Learn more: www.accenture.com


About the Role

You will be aligned with the Life Sciences R&D vertical, supporting services across the life sciences enterprise including:

  • Research laboratories

  • Clinical trials support

  • Regulatory services

  • Pharmacovigilance and patient services solutions

Within this, you will be part of the Clinical, Pharmacovigilance & Regulatory sub-offering, helping leading biopharma companies bring their vision to life by improving patient outcomes through scientific expertise and patient-centric insights.


Key Responsibilities

  • Manage the Affiliate Mailbox and perform reconciliation of reports as per defined processes.

  • Perform all written follow-up activities for both Serious and Non-serious cases.

  • Create and manage:

    • Case identification

    • Data entry

    • MedDRA coding

    • Case processing

    • Submission and follow-ups for ICSRs in the safety database, in line with client guidelines and global regulatory requirements.

  • Analyze and solve moderately complex problems, creating or adapting methods and procedures as required.

  • Provide input into team direction and ensure alignment with strategic goals set by senior management.

  • Interact with supervisors, peers, and client management as needed.

  • Manage small teams and/or specific work efforts (when not in an individual contributor role).

  • Work in rotational shifts as required.


What We’re Looking For

  • Strong knowledge and experience in Pharmacovigilance & Drug Safety Surveillance.

  • Ability to analyze and resolve moderately complex problems.

  • Capability to design new solutions or adapt existing ones.

  • Understanding of organizational strategy and its alignment with team goals.

  • Good interpersonal and communication skills for client and team interactions.

  • Leadership skills to guide small teams and manage deliverables effectively.

  • Flexibility to work in rotational shifts.


✅ This structured format highlights the role overview, key tasks, and requirements in a professional and easy-to-read way.