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Lifescience Regulatory Svs Associate

0-2 years
₹4.5 LPA to ₹6.5 LPA
10 June 12, 2025
Job Description
Job Type: Full Time Education: B.Pharm/M.Pharm 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 – Accenture | Bengaluru
Job No.: AIOC-S01584834
Employment Type: Full-time
Experience Required: 1 to 3 years
Location: Bengaluru

About the Role:
Accenture is seeking LifeScience Regulatory Services Associates to support its Life Sciences R&D vertical. This position involves critical regulatory operations responsibilities such as document formatting, submission preparation, and compliance support to ensure successful interactions with global health authorities. You'll contribute to delivering regulatory solutions that help top biopharma clients bring treatments to patients faster and more effectively.

Key Responsibilities:

  • Perform regulatory operations tasks such as bookmarking, hyperlinking, and document formatting in line with ICH and other global regulatory standards.

  • Conduct quality control (Document QC) checks to ensure submission readiness.

  • Review and transform source documents as per submission requirements.

  • Collate and evaluate scientific data generated during research and development.

  • Support in authoring CMC documents, building submission strategies, and preparing health authority packages.

  • Ensure regulatory compliance of products throughout their lifecycle.

  • Interpret and advise on relevant legal, scientific, and procedural regulations.

  • Work closely with internal teams and supervisors under detailed guidance.

  • Contribute to a collaborative environment with a narrow and focused scope of tasks.

  • Be open to rotational shifts as per project needs.

Required Skills:

  • Proficiency in regulatory documentation, QC processes, and document publishing standards.

  • Strong attention to detail and commitment to meeting deadlines.

  • Team-oriented mindset with adaptability and quick learning ability.

  • Basic understanding of pharmaceutical product development and regulatory frameworks.

Qualifications:

  • Bachelor of Pharmacy (BPharm) or Master of Pharmacy (MPharm)

  • 1 to 3 years of relevant experience in regulatory services or regulatory affairs

Why Join Accenture?

  • Be part of a team shaping the future of healthcare compliance and regulatory success.

  • Work with global leaders in biopharma and help bring critical products to market.

  • Access continuous training, professional growth, and world-class digital infrastructure.

Salary: ₹4.5 LPA to ₹6.5 LPA (estimated for 1–3 years experience in regulatory services)