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Pharmacovigilance Services Associate

0-2 years
Not Disclosed
10 Dec. 5, 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

Pharmacovigilance Services Associate

Location: Bengaluru, Karnataka, India
Employment Type: Full-Time
Experience Required: 0–2 years


Company Overview

Accenture is a global professional services leader with expertise in digital, cloud, and security solutions. With operations across more than 120 countries and a workforce of over 699,000 professionals, Accenture combines technology and human ingenuity to deliver innovative solutions in Strategy & Consulting, Technology & Operations, and Accenture Song.

Our Life Sciences R&D vertical supports the full spectrum of the industry, including research laboratories, clinical trial operations, regulatory services, pharmacovigilance, and patient services.


Role Overview

We are seeking a Pharmacovigilance Services Associate to join our Life Sciences team in Bengaluru. This entry-level position is ideal for Pharmacy graduates (B.Pharm/M.Pharm) with 0–2 years of experience in pharmacovigilance, safety writing, or drug safety operations.

The role involves managing adverse event reports, developing case narratives, and ensuring compliance with global regulatory requirements. You will work closely with your team and supervisors to support pharmacovigilance operations and contribute to the safety reporting process for clinical studies and regulatory submissions.


Key Responsibilities

  • Manage the Affiliate Mailbox and reconcile reports as per defined processes.

  • Perform follow-up on adverse events, including both serious and non-serious cases.

  • Develop individual case narratives for inclusion in safety reports and clinical study submissions.

  • Ensure compliance with global pharmacovigilance guidelines and internal SOPs.

  • Solve routine operational issues using established procedures and guidelines.

  • Collaborate with team members and escalate complex cases to supervisors.

  • Maintain accurate documentation and support regulatory audits when required.

  • Work in rotational shifts as needed.


Qualifications & Skills Required

  • Bachelor’s or Master’s degree in Pharmacy (B.Pharm/M.Pharm).

  • 0–2 years of experience in pharmacovigilance, drug safety, or regulatory reporting.

  • Knowledge of adverse event reporting, ICH-GCP, and pharmacovigilance operations.

  • Strong written and verbal communication skills in English.

  • Attention to detail, accuracy, and organizational skills.

  • Ability to work independently while supporting team objectives.


Why Join Accenture Life Sciences?

  • Gain hands-on experience in global pharmacovigilance operations.

  • Contribute to drug safety and patient care for leading biopharma companies.

  • Exposure to clinical study safety reporting, regulatory submissions, and compliance standards.

  • Collaborative and inclusive work environment with learning and career growth opportunities.

  • Opportunity to work with a global network of Life Sciences experts and advanced technologies.


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