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: Sr Clinical Research Associate/Clinical Research Associate

Location: Ahmedabad

Job Description:

  • Identify and qualify potential Investigators.
  • Responsible for identification & collection of necessary documents in order to check the feasibility of site/ investigator and approval from authorities.
  • Responsible for training of site study team, recording & maintenance of essential documents, and for startup activities & site initiation.
  • Conduct monitoring visits to check compliance with study management, protocol & other requirements at all assigned sites.
  • Perform source document verification as per monitoring plan and ensure that source documents & other trial records are accurate, complete, kept up-to-date & maintained according to applicable SOP’s to avoid incomplete records.
  • Responsible for study updates & Coordination with Labs & other trial-related services as per the study requirements.
  • Responsible for IP accountability and availability, tracking, and management of all Clinical Trial related supplies shipped to the sites/warehouse & accordingly clinical trials supplies vendor management for the study.
  • Responsible for site-closeout & follow up activities in order to maintain documents at the site.
  • Assist with the audit of an investigation site or central files and liaise with Quality Assurance personnel as required to ensure that the study is being conducted in accordance with ICH GCP and applicable regulatory guidelines.

Qualification: BAMS/BHMS, B.Pharma/B.Sc, MS/M.Sc

Experience: 1-6 Years

Salary: Negotiable

Contact Details:

dmirchandani@cliantha.com, careers@cliantha.comhr@cliantha.com

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