Navya Shree

I’m a Research Associate and Study Director with 4 years of non-clinical research experience in Bioassay and Chronic Toxicology, and I’m now transitioning into Clinical Research. I focus on maintaining data integrity, protocol compliance, and producing accurate, complete study documentation.

In my roles at Bioneeds Ind. Pvt. Ltd. (Aug 2020 – Sep 2023) and Adgyl life sciences (Nov 2023 – Sep 2025), I performed toxicokinetic and bioassay projects, including Insulin assays, antigenicity work, Menotropin assays, and Urofollitropin assays. I also supported repeat-dose toxicity studies (28-day, 90-day, and 6-month), DRF studies, and carcinogenicity studies in rodents.

I’m confident in GLP and regulatory concepts (OECD and FDA guidelines), and I contribute by meticulously reviewing and validating raw data and reports for accuracy. I prepare study plans and toxicology reports, work with dose formulation preparation, follow multiple dose routes, and apply SEND concepts for regulatory submissions.