Instagram
youtube
Facebook

Lifescience Regulatory Svs Associate

1-3 years
Not Disclosed
10 June 18, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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, Bangalore

Job Summary:

Accenture is hiring a LifeScience Regulatory Services Associate for its Bangalore office. This full-time, on-site position requires 1 to 3 years of experience in regulatory affairs within the life sciences industry. Ideal for B.Pharm or M.Pharm graduates, the role offers a chance to contribute to global regulatory submissions, CMC document preparation, and data evaluation for leading pharmaceutical clients.


Key Responsibilities:

  • Perform regulatory operations tasks including bookmarking, hyperlinking, and document formatting per ICH guidelines and Health Authorities’ requirements.

  • Review, transform, and quality-check submission documents (Document QC).

  • Collect, organize, and assess scientific data generated during R&D processes.

  • Provide guidance on scientific and legal regulatory requirements.

  • Develop regulatory submission strategies and author CMC documents and regulatory authority packages.

  • Ensure product compliance with current global regulations.

  • Participate in team-based tasks with routine problem-solving responsibilities.

  • Support the team with detailed guidance on new assignments and processes.


Required Skills & Qualifications:

  • Educational Qualification: Bachelor’s or Master’s degree in Pharmacy (B.Pharm/M.Pharm).

  • Experience: 1 to 3 years in life sciences regulatory affairs or related roles.

  • Strong understanding of ICH guidelines, regulatory submissions, and Health Authority requirements.

  • Ability to work under deadlines and perform quality checks on regulatory documents.

  • Detail-oriented, adaptable, and quick learner with team collaboration skills.

  • Strong analytical and problem-solving skills.

  • Excellent written and verbal communication abilities.

  • Flexibility to work in rotational shifts if required.


Perks & Benefits:

  • Opportunity to work with a global leader in digital, cloud, and security services.

  • Access to continuous learning, certifications, and professional development programs.

  • Inclusive and diverse work environment fostering innovation and creativity.

  • Competitive compensation package (exact salary not specified).

  • Comprehensive health and wellness benefits.


Company Description:

Accenture is a global professional services company recognized for its leadership in digital transformation, cloud, and security. With a workforce of over 775,000 employees worldwide, Accenture delivers cutting-edge solutions to clients across various industries, including life sciences, healthcare, and technology.


Work Mode:

On-site – Bangalore, India


Call to Action:

Ready to build your career in regulatory affairs with a global leader? Apply now to join Accenture’s Life Sciences Regulatory team and make an impact in the pharmaceutical industry.