Clinical Trials


Dr. Dharmesh Domadia - Associate VP, Global Clinical Operations.

Dr. Dharmesh Domadia has more than 15 years of Healthcare Industry experience. He holds an MD in Pharmacology from Government Medical College Surat. His clinical research experience including BA-BE studies, Phase I (NCE), Experimental Work, Biologics, Biosimilar, Patient Based PK studies, Clinical endpoint studies and Late Phase Studies. He has successfully managed various regulatory audits including FDA, MHRA, MCC, MHCW, ANVISA and DCGI.

Prior to joining Cliantha, he worked for Sunpharma, Veeda Clinical Research & Lambda Therapeutics Pvt. Ltd. In his last assignment with Lambda therapeutics was as a Associate – Vice President, Clinical Operations and responsible for the overall execution of Late Phase clinical operations in compliance with the applicable Global Regulatory standards and ICH-GCP


Dr. Chirag Shah - Head, Clinical Trials.

Dr. Chirag Shah has rich experience of more than 14 years in multi disciplinary area of Product development in Pharmaceutical, Biotech companies and in Clinical Research Organisation (CRO). His expertise includes in the set up of a new department, Global Project Management (Discovery & Clinical-Phase I-IV), Preclinical drug development, Regulatory affairs, Medical Services, Pharmalicensing, Financial Management, Systems development, Business Development and Marketing.

Prior to joining Cliantha Research, he has worked with leading Indian companies such as Cipla, Intas, Alembic, Nicholas Piramal, SIRO Clinpharm. Dr. Chirag Shah has a Ph.D in Pharmacy from Saurashtra University, Rajkot, India. He is also specialized in the Pharmaceutical Management (PGDPM) from IES’s Management College and Research Center, Mumbai with special focus on Marketing, Operation and Finance. He is an associate member of American College of Clinical Pharmacology (ACCP), American Society of Clinical Oncology (ASCO), Life member of Indian Pharmacological Society (IPS) and Drug Information Association (DIA).


Kunal Sehra - Sr. Project Manager, Clinical Trials.

Mr. Kunal Sehra brings 15 years of Clinical Research and Pharmaceutical industry experience with the last 9 years in Project Management. Mr. Sehra’s successes include the setup of a new department, Global Project Management, line management, regulatory affairs, medical services, financial management, system development, Business Development and Marketing. He has been involved in variety of therapeutic areas such as Oncology, Biosimilars, Cardiology, Dermatology, Psychiatric, Endocrinology and Vaccines.

Prior to Cliantha, Mr. Sehra worked with Ranbaxy Research Labs, Torrent Pharmaceutical and two leading CROs in India. Mr. Sehra received his second Master’s degree in regulatory affairs and drug development from Northeastern University, Boston, his first Master’s degree in Clinical Research as well as a Pharmacy degree from India. He is an associate member of American College of Clinical Pharmacology (ACCP), American Society of Clinical Oncology (ASCO) and Drug Information Association (DIA).


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