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1.0 - 5.0 years

0 Lacs

karnataka

On-site

As a LifeScience Regulatory Services Associate at Accenture, you will be part of the Life Sciences R&D vertical, contributing to regulatory services for leading biopharma companies. Your role will involve performing regulatory affairs LCM with Veeva skill set, submission in accordance with ICH guidelines, and reviewing and transforming source documents. Additionally, you will be responsible for performing Quality Control checks for all submission components, collecting and evaluating scientific data, advising on legal and scientific requirements, and ensuring compliance with current regulations. Key Responsibilities: - Perform regulatory affairs LCM with Veeva skill set of submission in acco...

Posted 3 weeks ago

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1.0 - 5.0 years

0 Lacs

karnataka

On-site

As a LifeScience Regulatory Services Associate at Accenture, you will be a part of the Life Sciences R&D vertical, offering services ranging from research laboratories, clinical trials support, regulatory services, to pharmacovigilance and patient services solutions. Your role will involve performing regulatory affairs LCM with Veeva skill set of submission in accordance with ICH guidelines and other Health Authorities. You will review and transform Source Documents, conduct Quality Control (Document QC) checks for all submission components, and collect, collate, and evaluate the scientific data gathered as part of R&D. Additionally, you will advise on legal and scientific restraints and req...

Posted 3 months ago

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