Open to opportunities

Muskan Kumari

@muskankumari3

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Pharmacy postgraduate with 6 months in regulatory affairs, driven to support compliant clinical trials.

India

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What I'm looking for

I’m looking to contribute to clinical research in a role where I can handle regulatory documentation, apply GCP standards, and help maintain ethical, accurate, compliant trial data from start to finish.

I’m a Pharmacy postgraduate (B.Pharm & M.Pharm) with 6 months of industry experience and a strong interest in clinical trials. I’m familiar with regulatory documentation and GCP guidelines, and I’m motivated by the goal of ensuring ethical standards, data accuracy, and compliance throughout the trial process.

In my Regulatory Affairs role, I helped prepare, format, and submit regulatory documents, and supported reviewing SOPs. I also assisted in keeping regulatory records organized and up to date, while managing databases and filing systems to keep documentation reliable and accessible.

I’ve also trained in Quality Control, learning about Quality Check (QC) of drugs and Quality Control Testing. I gained exposure to Instrument Calibration & Maintenance as well, and I bring that quality mindset into how I handle documentation and compliance for clinical work.

Experience

Work history, roles, and key accomplishments

Management Assistant, Regulatory Affairs

Rhydburg

Aug 2003 - Mar 2024 (20 years 7 months)

Supported the preparation, formatting, submission, and review of regulatory documents, including SOP-related support. Managed and maintained regulatory records, databases, and filing systems.

Regulatory Affairs Regulatory Documentation Database Management

Quality Control Training

IPCA

Jun 2023 - Jul 2023 (1 month)

Trained in Quality Control activities including quality checking of drugs and understanding instrument calibration and maintenance. Also covered regulatory documentation and GCP concepts during training.

Quality Control Regulatory Documentation GCP Word PowerPoint