Clinical Trial Nurse - Greenville, SC

pbspanJob Overview: Part time - 32-40 hours/wk and onsite support./span/bbr /spanCoordinate and participate in clinical research studies ensuring that studies are carried out according to/spanbr /spanprotocol, contracted scope of work, good clinical practice, sponsor standard operating/spanbr /spanprocedures (SOPs) and any relevant local guidelines and regulations./spanbr /spanEssential Functions/spanbr /span• Provides clinical research support to investigators to prepare for and execute assigned research studies/spanbr /span• Reviews study protocols, source document forms, other study-specific documents, and electronic data/spanbr /spancapture systems used to record clinical research data/spanbr /span• Collects and submits regulatory/ethics documentation as required by the Federal Drug Administration/spanbr /span(FDA) and other regulatory bodies governing the conduct of the study/spanbr /span• Recruits and screens patients for clinical trials and maintain subject screening and enrollment logs/spanbr /span• Orients research subjects to the study including the purpose of the study, procedures and protocol/spanbr /spanrequirements such as timeline for visits/spanbr /span• Maintains source documentation based on protocol requirements that adhere to Good Clinical Practice/spanbr /span(GCP)/International Conference on Harmonization (ICH) documentation principles/spanbr /span• Schedules and executes study visits and perform study procedures as delegated and supervised by the/spanbr /spanPrincipal Investigator/spanbr /span• Handles lab testing and analysis including preparation of specimen collection tubes and lab logistics/spanbr /span• Monitors subject safety and report adverse events and reactions to Principal Investigator, study team/spanbr /spanmembers and IRBs as appropriate/spanbr /span• Corresponds with research subjects to troubleshoot study-related questions or concerns/spanbr /span• Participates in routine meetings with site study staff and Investigators to confirm study tasks are assigned/spanbr /spanand are executed to the expected standards/spanbr /span• Actively involved in study data quality checking and query resolution/spanbr /span• Performs a variety of complex clinical research procedures including but not limited to electrocardiogram/spanbr /span(ECG), lab sample collection, spirometry, vital signs, dose verifications, cardiac telemetry monitoring, and/spanbr /spanquestionnaire administration/spanbr /span• Updates and maintains site staff skills, training and knowledge of current best nursing practices and topics/spanbr /spanrelated to clinical research/spanbr /span• Assists the investigators to safeguard the well-being of subjects and maintain standards required of/spanbr /spanclinical research sites/spanbr /span• Maintains a safe environment in accordance with site policies/spanbr /span• Acts as an advocate for research subjects/spanbr /span• Addresses subject questions in a pro-active manner and take remedial action as required/spanbr /span• Assists and advise site staff in nursing practices and on the delivery of study care to subjects/spanbr /span• Reports any deviations from normal research practices to senior staff and implement agreed changes in/spanbr /spanthe study care program/spanbr /span• Assists investigator in verifying that research study objectives are met on time, within budget and/spanbr /spanaccording to application protocol requirements, clinical research regulations and quality standards/spanbr /span• Assists in providing training to new investigator site staff members on study-specific topics and/spanbr /spanrequirements/spanbr /span• Maintains adherence to investigator site staff training requirements by auditing and maintaining training/spanbr /spanrecords/spanbr /span• Provides guidance and supervision to lower level site staff to help provide that processes are carried out/spanbr /spanin line with protocols and SOP#39;s, where applicable/spanbr /span• Participates in study process reviews and enhancement efforts to support control of site unit budget,/spanbr /spandevelopment of the research facilities and site services and the culture towards a high performing research/spanbr /spanstudy team/spanbr /span• Prepares for and attend study monitoring visits, study audits and regulatory inspections with clinical/spanbr /spanresearch regulatory agencies/spanbr /span• Adheres to standard operating procedures (SOPs) and other directives throughout this process/spanbr /span• Assists research site with coverage planning related to staffing and scheduling for research projec/span/pp/ppspanIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide/span. Learn more at a href="https://jobs.iqvia.com/" target="_blank"spanspanspanspanspanhttps://jobs.iqvia.com/span/span/span/span/span/a/pp/ppspanIQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. /spana href="https://jobs.iqvia.com/eoe" target="_blank"spanspanspanspanspanhttps://jobs.iqvia.com/eoe/span/span/span/span/span/a/pp/pp/pp/pp/pThe potential base pay range for this role is $50.00-$60.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.