Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Pharmacovigilance Services New Associate

Accenture
Accenture
0-2 years
Not Disclosed
Bengaluru, India
10 Feb. 17, 2026
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 Title: Pharmacovigilance Services New Associate
Location: Bengaluru, India
Job Type: Full-time
Experience Required: 0–2 years in Pharmacovigilance, Drug Safety, or Life Sciences domain
Job Reference: AIOC-S01628146

Company Overview
Accenture is a global professional services organization with leading capabilities in digital, cloud, and security solutions. With extensive expertise across more than 40 industries, Accenture provides services in Strategy and Consulting, Technology, and Operations. The organization operates one of the world’s largest networks of Advanced Technology and Intelligent Operations centers, serving clients in over 120 countries. Accenture focuses on driving innovation and delivering value by combining advanced technology with human expertise.

Within its Life Sciences Research and Development (R&D) division, Accenture supports pharmaceutical and biotechnology organizations through research support, clinical trial services, regulatory compliance, pharmacovigilance operations, and patient-centered solutions.

Job Overview
The Pharmacovigilance Services New Associate will support pharmacovigilance operations and drug safety surveillance activities to ensure the safety and regulatory compliance of pharmaceutical products. The role involves monitoring adverse drug reactions, managing safety data, and supporting case processing activities in accordance with global regulatory standards and client requirements.

This position is suitable for early-career professionals seeking to build expertise in pharmacovigilance, clinical safety, and regulatory operations within the life sciences industry.

Key Responsibilities

  • Perform pharmacovigilance and drug safety surveillance activities.

  • Create and manage case identification, data entry, and case processing for Individual Case Safety Reports (ICSRs).

  • Conduct medical coding using standardized terminology and maintain safety databases.

  • Process case submissions and perform follow-up activities according to client and regulatory guidelines.

  • Monitor, detect, and evaluate adverse drug reactions and safety information.

  • Support data collection and analysis from clinical trials, healthcare providers, and patients.

  • Ensure compliance with global pharmacovigilance regulations and quality standards.

  • Resolve routine operational issues by following established procedures and guidelines.

  • Collaborate with team members and supervisors to ensure timely task completion.

  • Maintain accurate documentation and ensure data integrity in all pharmacovigilance activities.

Qualifications and Eligibility

  • Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or related discipline (B.Pharm, M.Pharm, MSc).

  • 0–2 years of relevant experience in pharmacovigilance, drug safety, or clinical research operations.

  • Understanding of pharmacovigilance processes and regulatory requirements is preferred.

  • Strong analytical skills and attention to detail.

  • Good written and verbal communication skills.

  • Ability to work in a team-based environment with structured guidance.

  • Willingness to work in rotational shifts, if required.

Work Environment and Role Expectations

  • Entry-level role with structured training and detailed task instructions.

  • Individual contributor role within a defined scope of work.

  • Regular interaction with immediate team members and reporting managers.

  • Work performed under supervision with focus on accuracy and compliance.

Career Growth Opportunities
This role provides foundational experience in pharmacovigilance and drug safety operations, offering opportunities to develop expertise in clinical research, regulatory compliance, and pharmaceutical safety within a global life sciences environment.