Site Report Specialist (Clinical Trials)
Experience - 4 to 6 years as Site Report Specialist
Qualification - B.Pharm / M. Pharm / Pharm. D
Location - Ahmedabad
Interested candidates can send their resume at vdesai@cliantha.com | mjunnarkar@cliantha.com
Based in Ahmedabad, India, Cliantha Research are a full-service Clinical Research Organization (CRO) and a top supplier of clinical research services. The goal of Cliantha is Science with Integrity. 18 years of flawless regulatory history with the USFDA, WHO, MHRA, Health Canada, AGES, AEMPS, MCC, MOH, ANSM, MOPH, ANVISA, CAP, and NABL are all possessed by Cliantha. With offices in Ahmedabad, Noida, and Vadodara, Cliantha Research is based in India. Cliantha has operations in the United States (in Florida and New Jersey for project management), Canada (in Mississauga, Winnipeg, and Scarborough), and Portugal (In project management). In eighteen years, Cliantha has accumulated expertise in Early Phase (BA/BE), First in Man, Late Phase (various therapeutic areas), Respiratory, Tobacco Research, Dermatology, Consumer Research, Analytical lab, Diagnostic Central lab, IVRT, IVPT, Biometrics, Environmental Exposure Chambers and Medical Services.