Clinical Research Coordinator is Responsible for Conducting Trials as per the Gcp Guidelines Under the Supervision of the Principal Investigator (pi). Although the Pi Has the Overall Responsibility for Performing the Trial, It Has Been Stated that the Crc is the Heart and Soul of the Clinical Trial and That, Eventually, It is the Crc Who Carries Ahead the Research Objectives, in that Way Playing An Important Role in the Success of the Clinical Trial. Most Significantly, Crcs are Usually Engaged in Vital Duties that have Been Usually Carried Out By the Pi, Some of Them Being the Informed Consent Process and Making Sure that the Site Staff is in Compliance with the Crcs Main Responsibility, as with all Clinical Research Staff, is to Ensure the Protection and Well-being of the Patients Participating in the Study.
Experience : 0 - 1 Years
No. of Openings : 10
Education : B.Pharma, B.Sc, B.Tech/B.E, MBBS, MD/Medicine Doctor, Post Graduate Diploma, M.Pharma, M.Sc, Any Doctorate Degree, Ph.D/Doctorate
Role : Clinical Research Coordinator
Industry Type : Pharma / BioTech / Clinical Research
Gender : [ Male / Female ]
Job Country : India