Regional Clinical Research Associate - Southeast
Tech Observer - Charlotte, NC

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·Delivery of high quality data according to agreed timelines and budget, ensuring adherence to
international and local regulations and Company SOP standards
·Demonstrate exceptional customer focus as evidenced by positive feedback from Company
colleagues and external customers (Investigators)
·Participate in the site nomination process; perform evaluation of site capability to deliver the
contractually agreed to number of patients and high quality data then make recommendation for
inclusion in the clinical trial
·Assume ambassadorial role to facilitate communication between sites and Company line
functions to increase value proposition to investigators
·Facilitate preparation and collection of site level documents
·Execute site initiation and training activities
·Perform monitoring visits according to monitoring plan and author study monitoring reports
·Manage site drug supply management
·Resolve site level update of technical systems (ClinAdmin, EDC)
·Ensure site activities in line with milestones (i.e. startup, recruitment, closeout, etc)
·Manage recruitment implementing appropriate contingency plans as needed
·Assure continual GCP, ICH and Company SOP compliance (Informed consent process, source
data verification, AE and SAE reporting, IN, protocol, drug accountability etc.)
·Resolve deviations to standard by remedial action and training
·Perform data query resolution process (both at Site and with Data Management)
·Execute site closeout activities
·May act as local (or global) CRA Lead, as assigned. May act as a mentor to new associates for
purposes of field training, as assigned

·Industry experience necessary - no Coordinators for this role will be considered at this time
·Basic medical and business knowledge
·Desired competency in clinical research or having demonstrated adequate level of proficiency
within the CRA II competency profile
·Understands and can apply knowledge of clinical trial designs to trial execution
·Knowledge and experience in international standards (GCP/ICH), international (FDA, EMEA) and
local regulations
·Expertise in communication, managing multiple priorities and computer literacy

·A degree in a scientific or health care discipline preferred

(SITE LOCATIONS: Florida, North Carolina, South Carolina - Candidate must live in this area, not just willing to travel to it. No relocation arrangements will be considered.)

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