Cliantha Research, a full-service Clinical Research Organization (CRO), is a leading provider of Clinical research services, based in Ahmedabad, India. Cliantha’s mission 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.

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Cliantha Research is headquartered in India with facilities in Ahmedabad, Noida, and Vadodara. Cliantha has a presence in the USA (facilities in Florida and Project Management in New Jersey), Canada (facilities in Mississauga, Winnipeg, and Scarborough), and Portugal (Project management).

In fifteen 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.

Position: Principal Investigator

Location: Sect – 63, Noida, Uttar Pradesh

Job Description:

  • Monitoring and reporting of clinical trial-related activities
  • Communication and coordination of study-related activities
  • To check and review the raw data
  • To ensure that the studies are carried out as per protocol and applicable regulatory requirements of GCP
  • To provide protocol training to all paramedical staff.
  • ICF presentation to volunteers and answer queries
  • To monitor vitals and adverse events during the study
  • To conduct the clinical examination of all subjects participating during all clinical Studies
  • To assist in the accurate compilation of raw data
  • To provide assistance in the compilation of clinical reports
  • Protocol training & delegation of study activities to the study team.

Qualification: MBBS Freshers/Exp in CRO/Hospital

Experience: 0-3 Years

Salary: Negotiable

Contact Details:

hrnoida@cliantha.com

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