Job Title: LifeScience Regulatory Services Analyst
Location: Bengaluru, India
Job Type: Full-Time
Experience Required: 2–5 Years
Functional Area: Regulatory Affairs / Life Sciences
Company Overview
Accenture is a global leader in professional services, combining digital, cloud, and security capabilities with deep industry expertise. Serving clients across 40+ industries, Accenture delivers strategy, consulting, technology, and operations solutions to drive innovation and operational excellence. With a workforce of 699,000 professionals worldwide, we empower organizations to transform efficiently and create lasting value.
Role Overview
We are seeking a LifeScience Regulatory Services Analyst to support our Life Sciences R&D vertical. This role focuses on regulatory compliance, electronic submission management, and documentation support for global biopharmaceutical clients. The ideal candidate will have a B.Pharm degree and experience in regulatory operations, contributing to the preparation and management of filings, lifecycle submissions, and compliance tracking.
Key Responsibilities
Coordinate and manage documentation required for global regulatory submissions.
Prepare and process electronic submissions including original applications, lifecycle management submissions (CMC, ad-promos, amendments, annual reports, SPLs, etc.).
Analyze and resolve low-to-moderate complexity regulatory issues following SOPs and guidelines.
Collaborate with peers and supervisors to ensure regulatory compliance and productivity benefits.
Maintain accurate trackers, reports, and regulatory databases.
Function as an individual contributor with a focused scope of work.
Adapt to rotational shifts as required to support global operations.
Qualifications & Experience
Education: Bachelor of Pharmacy (B.Pharm).
Experience: 2–5 years in regulatory affairs or life sciences operations.
Strong analytical and problem-solving skills.
Ability to work independently and collaboratively within a team.
Excellent attention to detail, organization, and communication skills.
Familiarity with global regulatory requirements and submission processes preferred.
Why Join Accenture
Gain exposure to global life sciences regulatory operations and compliance processes.
Work with leading biopharma clients on regulatory lifecycle management and submissions.
Access learning, mentorship, and career advancement opportunities in a dynamic environment.
Be part of a diverse and inclusive workplace that encourages innovation and growth.
Equal Opportunity Employer
Accenture is committed to providing equal employment opportunities without regard to age, race, religion, gender, disability, or any other legally protected status.
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