Accenture Recruitment LifeScience Regulatory Svs Associate

Accenture, a global leader in digital, cloud, and security services, is seeking a qualified LifeScience Regulatory Services Associate for its Bengaluru office. This role is ideal for individuals with a Bachelor’s or Master’s degree in Pharmacy and 1 to 3 years of experience in regulatory operations within the pharmaceutical industry.

About Accenture:

Accenture is renowned for its expertise across 40+ industries, offering Strategy and Consulting, Technology, and Operations services. With a workforce of over 699,000 professionals worldwide, Accenture empowers clients in more than 120 countries to achieve transformative outcomes through technology and human ingenuity.

Job Description:

As a LifeScience Regulatory Services Associate at Accenture, you will be part of the Life Sciences R&D vertical, supporting services ranging from research and clinical trials to regulatory compliance and patient services. Your responsibilities will include:

  • Managing regulatory operations tasks such as bookmarking, hyper linking, and transforming source documents in compliance with ICH guidelines and Health Authority regulations.
  • Performing Quality Control (Document QC) checks for submission components and coordinating essential documentation for global applications.
  • Processing electronic submissions, including original applications, CMC submissions, amendments, annual reports, SPL submissions, and more.
Accenture recruitment LifeScience Regulatory Svs Associate
Accenture recruitment LifeScience Regulatory Svs Associate

Qualifications and Skills:

To excel in this role, you should possess:

  • Problem-solving and analytical skills.
  • Commitment to maintaining high-quality standards.
  • A Bachelor’s or Master’s degree in Pharmacy.

How to Apply:

Ready to join Accenture’s dynamic team in Bengaluru? Apply online through the official Accenture Careers portal using the following link: Accenture Recruitment: LifeScience Regulatory Services Associate

To apply for this job please visit

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