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Are you looking to build your career in Life Sciences Regulatory Affairs? Accenture, a global leader in professional services, is hiring a LifeScience Regulatory Services Associate in Bengaluru. This role offers an exciting opportunity for freshers and early-career professionals (0–2 years) with a Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm) degree.
As part of Accenture’s Life Sciences R&D vertical, you will work on regulatory services, clinical trials support, pharmacovigilance, and compliance, helping top biopharma companies bring their vision to life.
Key Responsibilities
As a LifeScience Regulatory Svs Associate, you will:
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- Perform regulatory operations tasks such as bookmarking and hyperlinking for submission components.
- Review and transform source documents in line with ICH guidelines and Health Authority standards.
- Conduct Quality Control (Document QC) checks on all submission components.
- Collect, collate, and evaluate scientific data from R&D activities.
- Support in building regulatory submission strategies and authoring CMC documents.
- Ensure compliance with legal, scientific, and regulatory requirements.
- Collaborate with cross-functional teams under supervision and follow detailed work instructions.
Qualifications & Skills Required
- Education: B.Pharm / M.Pharm
- Experience: 0–2 years (freshers can apply)
- Skills:
- Strong attention to detail and ability to meet deadlines.
- Flexibility and adaptability in a dynamic work environment.
- Team collaboration skills.
- Quick learner with problem-solving abilities.
Benefits of Joining Accenture
- Opportunity to work with global biopharma leaders.
- Exposure to cutting-edge regulatory technologies.
- Career growth within Life Sciences Regulatory Services.
- Structured learning and mentoring support.
- Competitive salary package and shift allowances (rotational shifts may apply).
How to Apply
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