Dr. Snehasis Jana - Academia.edu (original) (raw)

I am an adroit, competent & diligent professional with experience of 11 years across the biopharmaceutical industries/CRO viz. Ranbaxy Research Lab, Syngene International Ltd, Sai Advantium Pharma Ltd, and Laila Nutraceuticals, India. I adept at performing technical, analytical duties for various type of new drug discovery and development projects; well versed in preclinical formulation development tasks and clinical trial procedures, protocol and other relevant regulatory requirements like ICH, OECD, EMEA, FDA and MIST guidelines for documentation of safety and toxicity data and reports for IND filing for FDA approval.
I have a strong theoretical and technical expertise in a range of in vitro and in-vivo efficacy Pharmacology, in vitro and in-vivo DMPK, radio labeled ADME studies, microbiology and in vitro and in-vivo regulated Toxicology studies. I am well versed with analytical and bioanalysis of bio-samples such as blood, plasma, CSF, tissues (brain, liver, kidney & lung), urine and feces using HPLC, UPLC and LC-MS/MS and also have in depth work experience to validate dried blood spot (DBT) analysis technique. I have excellent skills to develop various types of formulations in preclinical drug discovery set up for poorly aqueous soluble compounds.

I have been part of various Bio/pharmaceuticals/ Nutraceuticals discovery and development projects for various products in different therapeutic areas such as biosimilars for anti-cancers (hG-CSF and hGM-CSF), Immuno-oncology, anti-inflammatory, CNS targets, pro-drug projects, cardiovascular, metabolic disorders (diabetes and Obesity, dyslipidemia), anti-malarials (MMV i.e Medicines for Malaria Venture), anti-infectives, anti-retroviral, Nutraceuticals & herbal supplements etc. as a scientific group leader/ scientific manager.
Supervisors: Mahendra Kumar Trivedi and Trivedi Effect

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