Skill required: Regulatory Services - Clinical & Regulatory Writing
Designation: LifeScience Regulatory Svs Sr Analyst
Qualifications:Master of Pharmacy
Years of Experience:5 to 8 years
About Accenture
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What would you do? • Assist with data collection and initial drafting of Chemistry, Manufacturing, and Controls (CMC) documents.




• Collaborate with team members to ensure accuracy and completeness of regulatory submissions.

• The incumbent will perform the regulatory operations tasks of bookmarking and hyper linking for granular components documents of submission in accordance with ICH guidelines and other Health Authorities review and transform Source Documents Perform Quality Control Document QC checks for all submission components

• Produce variety of clinical documents throughout the lifecycle of a (potential) treatment, starting with describing and reporting data from clinical trials, through to preparing regulatory submission documents including post approval reports.
What are we looking for? • Primary skill - Clinical & Regulatory Writing - P5
• Maintain records of CMC authoring activities in alignment with organizational standards.
• Have understanding on Veeva RIMS and DMS
Roles and Responsibilities: • In this role you are required to do analysis and solving of increasingly complex problems.

📌 LifeScience Regulatory Svs Sr Analyst (Bengaluru)
🏢 Accenture
📍 Bengaluru