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    Regulatory Services Associate at Accenture Careers | Apply Now

    Launch Your Regulatory Affairs Career – LifeScience Regulatory Associate Role

    Begin your journey with Accenture Careers through this exciting LifeScience Regulatory Services Associate position designed for freshers and early professionals looking to grow in Regulatory Affairs Jobs. This role offers hands-on experience in regulatory submissions, document publishing, quality control, and life sciences compliance—making it a strong entry point for those aspiring to build a successful career in global regulatory operations.

    Job Details:

    • Job Title: LifeScience Regulatory Svs Associate
    • Experience: 0-2 years
    • Job No. AIOC-S01615323
    • Location: Bengaluru

    About the Company:

    Accenture is a global professional services company with leading capabilities in digital, cloud, and security. With unmatched experience across 40+ industries, Accenture delivers Strategy and Consulting, Technology and Operations services, and Accenture Song. More than 699,000 employees bring innovation and human ingenuity to clients in 120+ countries.

    Accenture invests heavily in research and development, supported by global innovation centers, life sciences labs, intelligent operations hubs, and advanced technology facilities. Their life sciences operations—where roles like Regulatory Affairs Jobs fall—focus on regulatory compliance, clinical development support, pharmacovigilance, and digital patient engagement solutions for leading global biopharma organizations.

    Job Description:

    You will be aligned with the Life Sciences R&D vertical. The work includes support across research labs, clinical trial support, regulatory services, and pharmacovigilance. Employees help leading biopharma companies improve outcomes by connecting scientific expertise with deep insights into the patient experience. Responsibilities include regulatory operations tasks such as bookmarking, hyperlinking, quality checks, transforming source documents, and managing global submissions—covering CMC, lifecycle management, amendments, ad-promos, SPL submissions, and more.

    Key Responsibilities at Accenture Careers:

    • Solve routine problems through set guidelines, Ideal For regulatory affairs jobs.
    • Work closely with your team and supervisor.
    • Follow detailed instruction for daily tasks and new assignments.
    • Make decisions impacting your own work.
    • Contribute as an individual within a team structure.
    • Role may require rotational shifts.

    Qualification Required for Accenture Careers:

    • Bachelor of Pharmacy
    • Preferably less than one year of experience in eCTD publishing or document publishing.

    CLICK HERE TO APPLY

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