LifeScience Regulatory Services Associate – Bengaluru, India
Category: Regulatory Services | Life Sciences
Experience Required: 0–2 years
Employment Type: Full-Time
Location: Bengaluru, Karnataka, India
Job ID: AIOC-S01634595
About Accenture
Accenture is a global professional services leader with expertise in digital, cloud, and security. Serving clients across 40+ industries in over 120 countries, Accenture combines technology and human ingenuity to deliver innovative solutions. With a workforce of 784,000, we enable organizations to transform and achieve measurable results. Visit www.accenture.com to learn more.
Role Overview
As a LifeScience Regulatory Services Associate, you will join Accenture’s Life Sciences R&D vertical. This role is focused on regulatory operations, supporting global biopharma clients in compliance, documentation, and regulatory submissions. You will coordinate essential documentation, manage electronic submissions, and ensure lifecycle management compliance, including CMC filings, amendments, annual reports, SPL submissions, and promotional material reviews.
Key Responsibilities
Support regulatory submissions and documentation for global applications, ensuring accuracy and compliance
Manage electronic submission platforms and track lifecycle management activities
Stay updated on global regulatory requirements and industry guidelines
Conduct routine problem-solving within defined regulatory processes
Collaborate with internal teams and supervisors to ensure timely completion of tasks
Maintain records, trackers, and communication with regulatory authorities
Contribute as an individual contributor within a structured team environment
May involve rotational shifts depending on project requirements
Qualifications & Skills
Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm)
0–2 years of experience in regulatory affairs, life sciences, or pharmaceutical operations
Proficient in English (International) communication
Basic understanding of regulatory submission processes and compliance requirements
Strong attention to detail, organizational skills, and ability to follow SOPs
Why Join Accenture
Work with leading global biopharma companies and gain exposure to international regulatory standards
Opportunity to develop expertise in regulatory operations, electronic submissions, and compliance audits
Dynamic, collaborative, and innovative work environment with learning opportunities and career growth
How to Apply
Upload your CV online by clicking on Apply. Ensure all relevant qualifications and experience details are included.
Accenture is an Equal Opportunity Employer – All qualified applicants will receive consideration without regard to race, gender, disability, or any protected characteristics.
Deadline: Open until filled
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