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Lifescience Regulatory Svs Associate

Accenture
Accenture
0-2 years
Not Disclosed
Bengaluru, India
10 May 11, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title

Life Science Regulatory Services Associate

Job ID

AIOC-S01624477

Location

Bengaluru, India

Employment Type

Full-time

Experience Required

0–2 years (preferred 1–3 years)

Qualification

  • Bachelor of Pharmacy (B.Pharm)

  • Master of Pharmacy (M.Pharm)


About the Company

Accenture is a global professional services organization offering services in strategy, consulting, technology, and operations. It operates across 120+ countries and serves clients in more than 40 industries, supported by its large-scale digital and intelligent operations network.


Business Unit / Domain

Life Sciences R&D – Regulatory Services

This role is part of Accenture’s Life Sciences vertical, supporting pharmaceutical and biopharma companies across:

  • Research laboratories

  • Clinical trials support

  • Regulatory services

  • Pharmacovigilance

  • Patient services solutions


Role Overview

As a Regulatory Services Associate, you will support compliance and regulatory operations for life sciences organizations. Your responsibilities will focus on ensuring that global regulatory requirements are met through accurate documentation, submissions, and lifecycle management activities.


Key Responsibilities

  • Support regulatory compliance activities across life sciences operations

  • Prepare and manage documentation for global regulatory submissions

  • Handle electronic submissions including:

    • Original application filings

    • CMC (Chemistry, Manufacturing & Controls) submissions

    • Advertising & promotional materials (Ad-Promos)

    • Amendments and annual reports

    • SPL submissions (Structured Product Labeling)

  • Coordinate required documentation and resources for regulatory filings

  • Monitor and stay updated on regulatory changes

  • Assist in compliance checks and audits

  • Ensure timely and accurate submission to regulatory authorities


Required Skills

  • Knowledge of Life Sciences Regulatory Operations

  • Experience or exposure to:

    • Veeva systems

    • Docubridge publishing tool

  • Understanding of regulatory submission processes

  • Basic knowledge of compliance frameworks in pharma/life sciences


Work Expectations

  • Work as an individual contributor within a team

  • Handle routine problems using standard guidelines

  • Receive detailed instructions for tasks and new assignments

  • Limited decision-making impact (focused scope of work)

  • Interaction mainly within team and reporting manager

  • May require rotational shifts


About the Role Environment

  • Structured entry-level regulatory operations role

  • Focus on learning and execution of standard regulatory processes

  • Exposure to global regulatory submission systems and workflows


Equal Employment Opportunity

Accenture provides equal employment opportunities regardless of:

  • Age, gender, race, religion, disability, sexual orientation, or other protected categories


Important Notice (Fraud Alert)

  • Accenture does not charge any fee for employment

  • Candidates should not make any payments for job offers

  • Report fraudulent communication to: india.fc.check@accenture.com