Clinical Research Coordinator, On-Site, View, UT

Position: Clinical Research Coordinator, On-Site, Pleasant View, UT
Clinical Research Coordinator, On-Site, Pleasant View, UT page is loaded## Clinical Research Coordinator, On-Site, Pleasant View, UT locations:
Pleasant View, UT, United States of America time type:
Full time posted on:
Posted Yesterday job requisition :
R1524909
** Job Overview
** Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and/or seeking enrollment in clinical studies according to the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP).  Assist with daily workload planning.
** Essential Functions
** Provide clinical research support to investigators to prepare for and execute assigned research studies, including:
* Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data
* Attend all relevant study meetings
* Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research
* Recruit and screen patients for clinical trials and maintain subject screening logs
* Orient research subjects to the study, including the purpose of the study, procedures, and protocol issues such as timelines for visits
* Design and maintain source documentation based on protocol requirements;
* Schedule and execute study visits and perform study procedures
* Collect, record and maintain research subject study data according to study protocol and SOPs, preserving quality control for content, accuracy and completeness
* Handle lab testing and analysis, including preparation of specimen collection tubes and lab logistics
* Monitor subject safety and report adverse reactions to appropriate medical personnel
* Correspond with research subjects and troubleshoot study-related questions or issues
* Participate in “huddles” to confirm daily study tasks are assigned to team members and are executed to the expected standards
* Assist with study data quality checking and query resolution.
* Perform a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation and cardiac telemetry monitoring.
* • Record, report and interpret study findings appropriately to develop a study-specific database.
* Assist investigator in verifying that research study objectives are met on time, within budget and according to applicable protocol requirements, clinical research regulations and quality standards.
* Provide training to new investigator site staff members on study-specific topics and requirements.  Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records.
* Prepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies.
* Assist research site with coverage planning related to staffing and scheduling for research projects.
** Qualifications
* ** Bachelor's Degree Or High School Diploma or equivalent industry experience
* 3 years’  relevant work experience in a clinical environment or medical setting, e.g., medical assistant, assistant nurse, laboratory technician; or equivalent combination of education, training and experience Req
* Working knowledge of clinical trials
* Working knowledge of the principles of Good Clinical Practices (GCP)
* In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
* Skill in carrying out required clinical procedures such as intravenous catheter insertion and spirometry testing
* Good skill in using MS Windows and Office applications such as Access, Outlook and Word
* Excellent interpersonal skills
* Ability to pay close attention to detail
* Ability to establish and maintain effective working relationships with coworkers, managers and clients
* Applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies

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