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Roles and Responsibilities Performs review of clinical monitoring visit reports for allocated projects ensuring consistency across protocols and/or regions and escalates any protocol, site, and/or ... view more

Job description Job Description Your responsibilities include, but are not limited to: Act as monitor of specific sites on a clinical study, under supervision, as appropriate. Facilitate preparation ... view more

Required Experience Clinical Research Trainers Capable of delivering classroom training Working knowledge of ICH GCP guidline,CRA & CRC Strictly for Experience Clinical Research Professionals Onl ... view more

Site File Associate (eTMF)

Roles and Responsibilities Review site-level documentation to ensure compliance with GCP and IQVIA Biotechs standard operating procedures from maintenance through a close-out phase. Reviews inves ... view more

RESPONSIBILITIES: Perform Site Identification and conduct Feasibility Studies. Perform Site Selection Visit, Site Initiation Visits in accordance with the protocol and other applicable regulatory gu ... view more

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