Cliantha Research, a full-service Clinical Research Organization (CRO), is a leading provider of Clinical research services, based in Ahmedabad, India. Cliantha’s motto is Science with Integrity. Cliantha has fifteen years of impeccable regulatory history with USFDA, WHO, MHRA, Health Canada, AGES, AEMPS, MCC, MOH, ANSM, MOPH, ANVISA, CAP, and NABL.
Department - Clinical Trials
Qualification : B. Pharm / M. Sc / M. Pharm
Clinical Trial Lead
6 to 8 years onsite monitoring
Sr. Clinical Research associate
4 to 6 years onsite monitoring
Clinical Research Associate II
2 to 4 years onsite monitoring
Clinical Research Associate I
1 to 2 years onsite monitoring
Clinical Data Management
2 to 6 years of Core CDM Experience
Clinical Data Management
6 to 10 years of Core CDM Experience
Statistical Programmer
2 to 4 years of core SAS Programming Experience in Late Phase
Interested candidates can send their resume to mjunnarkar@cliantha.com, vdesai@cliantha.com
Last Date : 20th April, 2023
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