LifeScience Regulatory Svs Associate Accenture

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 requirements, ensuring the organization's products comply with current regulations. To excel in this role, you should possess skills in problem-solving, detail orientation, results orientation, strong analytical skills, and Life Sciences Automation Enablement. Your responsibilities will include solving routine problems, following general guidelines, and receiving detailed to moderate level of instruction on daily work tasks and new assignments. Your interactions will primarily be within your team and direct supervisor, and the decisions you make will impact your own work. You will be an individual contributor within a team, focusing on predetermined tasks. Please note that this role may require you to work in rotational shifts. To be eligible for this position, you should have a Master of Pharmacy degree and 1 to 3 years of relevant experience in regulatory services within the life sciences industry. Join Accenture, a global professional services company with expertise in digital, cloud, and security, and contribute to improving outcomes for the world's leading biopharma companies.,

Posted 4 days ago

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