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Lifescience Regulatory Svs Associate

1-3 years
Not Disclosed
10 July 29, 2025
Job Description
Job Type: Full Time Education: Master’s degree 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

 

LifeScience Regulatory Services Associate – Bengaluru (Full-Time)

Job Summary

Accenture is hiring a LifeScience Regulatory Services Associate to support its Regulatory Affairs operations in the Life Sciences domain. This role is best suited for Master of Pharmacy graduates with 1 to 3 years of experience in regulatory operations, submission formatting, and compliance activities. You'll contribute to helping top biopharma clients comply with ICH and health authority standards, ensuring smooth document handling and regulatory documentation.


Key Responsibilities

  • Perform bookmarking, hyperlinking, and document formatting for regulatory submissions

  • Conduct document-level Quality Control (QC) for all submission components

  • Review and transform source documents as per regulatory guidelines

  • Collect, organize, and evaluate scientific and R&D data

  • Ensure regulatory compliance with ICH and other global standards

  • Contribute to the creation of submission strategies, CMC documents, and authority packages

  • Collaborate with internal teams and regulatory professionals to maintain compliance

  • Handle document tracking, lifecycle management, and metadata updates


Required Skills & Qualifications

  • Master of Pharmacy (M.Pharm) degree (required)

  • 1 to 3 years of experience in regulatory affairs or regulatory operations

  • Working knowledge of ICH guidelines and regulatory documentation best practices

  • Attention to detail in document formatting and quality control

  • Ability to work under pressure and meet tight deadlines

  • Adaptability to rotational shifts and team-based workflows

  • Good communication and client interaction skills

  • Familiarity with Life Sciences R&D and global health authority requirements


Perks & Benefits

  • Exposure to global pharmaceutical regulatory projects

  • Skill-building opportunities and learning platforms

  • Inclusive and innovation-driven work culture

  • Comprehensive health and wellness support

  • Work-life balance with structured shift patterns

  • Opportunity to grow within Accenture's global operations network


Salary/Compensation Range

Not disclosed in the job description. Compensation will be based on experience and internal policies.


Company Description

Accenture is a global leader in professional services, combining digital transformation, operations, and life sciences expertise. With over 775,000 employees worldwide, Accenture empowers pharmaceutical and healthcare clients through regulatory consulting, tech innovation, and patient-centric services.


Work Mode

On-site – Based in Bengaluru, India
(Rotational shifts may apply)


Call to Action

Start your regulatory career with a global leader in life sciences operations.
Apply now to join Accenture as a Regulatory Services Associate in Bengaluru.