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Pharmacovigilance Services Sr Analyst

2-5 years
Not Disclosed
10 July 3, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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

 

Pharmacovigilance Services Senior Analyst – Bengaluru

Job Summary:
Accenture is hiring a skilled Pharmacovigilance Services Senior Analyst for its Bengaluru location. In this role, you'll be responsible for end-to-end case processing of ICSRs, including MedDRA coding, data entry, and regulatory submissions in alignment with global pharmacovigilance standards. This position offers a unique opportunity to work at the intersection of clinical research and drug safety while contributing to patient well-being through regulatory compliance and medical data analysis.


Key Responsibilities:

  • Perform case identification, data entry, MedDRA coding, case processing, and submission of ICSRs

  • Handle reconciliation of safety reports and manage affiliate mailbox activities

  • Conduct written follow-ups for both serious and non-serious adverse event cases

  • Ensure compliance with client-specific guidelines and global regulatory standards

  • Collaborate with internal teams and clients to ensure timely and accurate reporting

  • Solve moderately complex issues and contribute to process improvement

  • May supervise small teams or projects as needed

  • Work in rotational shifts as per project demands


Required Skills & Qualifications:

  • Bachelor's degree in Pharmacy (B.Pharm)

  • 5 to 8 years of experience in pharmacovigilance or drug safety

  • Strong knowledge of ICSR processing and pharmacovigilance workflows

  • Hands-on experience with MedDRA coding and safety databases

  • Good analytical and problem-solving skills

  • Excellent interpersonal and collaboration skills

  • Familiarity with global regulatory requirements and ICH-GCP guidelines

  • Ability to work independently with minimal supervision


Perks & Benefits:

  • Competitive salary and performance-linked bonuses

  • Learning and upskilling opportunities through internal training

  • Comprehensive health and wellness support

  • Inclusion in a global, diverse work culture

  • Access to advanced digital tools and platforms

  • Work-life balance with structured shift policies


Company Description:

Accenture is a global leader in digital, cloud, and security services, delivering innovative healthcare and life sciences solutions. With a dedicated Life Sciences R&D division, Accenture supports top biopharma companies in regulatory affairs, pharmacovigilance, clinical trials, and patient services.


Work Mode: On-site (Bengaluru, India)
Experience Level: 5–8 years
Job Type: Full-time, Permanent
Compensation Range: Not specified in the job description


Call to Action:

If you're passionate about drug safety and want to build your career with one of the world’s most innovative healthcare partners, apply now to join Accenture’s pharmacovigilance team in Bengaluru. Your expertise can make a real difference in patient outcomes and regulatory compliance.