Research Coordinator Neonatal - Sharp Mary Birch - Day Shift - Full Time - Full-time

pubHours/b/ub:/b/pp/ppbShift Start Time:/b/pVariablep style="text-align:left"bShift End Time:/b/pVariablep/pp/pp/ppbAWS Hours Requirement:/b/p8/40 - 8 Hour Shiftp/pp/pp/pp style="text-align:left"bAdditional Shift Information:/b/pp/pp/pp/pp style="text-align:left"bWeekend Requirements:/b/pAs Neededp/pp/pp/pp style="text-align:left"bOn-Call Required:/b/pNop style="text-align:inherit"/pp style="text-align:inherit"/pp style="text-align:inherit"/pp style="text-align:left"bHourly Pay Range (Minimum - Midpoint - Maximum):/b/p$42.790 - $55.210 - $61.840p style="text-align:inherit"br / /pp style="text-align:left"spanspanThe stated pay scale reflects the range that Sharp reasonably expects to pay for this position.  The actual pay rate and pay grade for this position will be dependent on a variety of factors, including an applicant’s years of experience, unique skills and abilities, education, alignment with similar internal candidates, marketplace factors, other requirements for the position, and employer business practices./span/spanspan /span/pp style="text-align:inherit"br / /pbrbWhat You Will Do/bbrOrganizes and coordinates neonatal clinical research studies from IRB/FDA approved protocols. Performs clinical research studies in compliance with GCP/ICH adherence. Provides research support to Sharp neonatologists in their role as investigators and/or sub-investigators; sharing in the responsibility for successful completion of clinical research studies at Sharp. Maintains working knowledge of assigned research projects and facilitates their success.brbrbRequired Qualifications/bulliBachelor's Degree In healthcare related field or Registered Respiratory Therapist (RRT). /lili5 Years Experience in a related field. /li li Experienced with good clinical practice techniques and accurate documentation. /li/ulbrbPreferred Qualifications/bulliCertified Clinical Research Coordinator (CCRC-ACRP) - The Association of Clinical Research Professionals -PREFERRED/li/ulbrbOther Qualification Requirements/bulliRegistered Respiratory Therapist (RRT) or Bachelor's degree in healthcare related field required./li/ulbrbEssential Functions/bbrul liCommunication and teamworkbrScreens, recruits, and evaluates patients for participation in studies per research protocols.brActs as a liaison between the patients, hospital, physicians and study personnel during implementation of assigned studies.brValidates understanding of coordination of plan of care and is responsive to questions or concerns.brSchedules patient visits, study procedures, and sponsor site visits.brDocuments telephone communications between the investigative (research) site and the study sponsors.brCoordinates and communicates progress of research protocols.brValidates patients#39; and families#39; understanding of plan care./li liPatient and family advocatebrValidates patient#39;s understanding of study protocols and objectives.brAssists the patient with study-related requirements and procedures.brParticipates in the informed consent process.brConsiders patient#39;s perspective about research studies, procedures, problems and issues, responding appropriately to their needs.brPatients#39; perceive as responsive, caring and effective.brPromotes the experience of participating in an out-patient or in-patient research study requiring RN scope of practice./li liPromotes and advocated research in discovery of best practicesbrKnowledgeable regarding current clinical practices and protocols, including eligibility criteria.brContributes to evaluating desirability and feasibility of participating in new research studies by representing Sharp Clinical Research programs at nationwide investigator meetings.brActs as a protocol resource person for specialists and clinical staff participating in research studies.brImplements patient recruitment strategies.brElicits and shares research study updates and results, interfacing with investigators and site coordinators at participating institutions nationwide./li liResearch managementbrEvaluates the patient at research study visits and communicates findings to the physician investigator.brConducts or delegates chart reviews to evaluate compliance with and results of study.brEnsures completion of principal investigators and sponsor#39;s research data queries per deadlines.brProvides clinical research monitors with required documents per site visit.brPrepares long-term storage for study records after research study is completed./li liResearch study implementationbrAssists the investigator in obtaining the required contracted patient enrollment for each study, using the protocol#39;s inclusion/exclusion criteria.brValidates clinical staff#39;s understanding of responsibilities related to research protocol implementation and documentation.brMonitors implementation of study protocols per IRB standards and study parameters.brDispenses and controls all research study drugs per FDA regulations.brPerforms study-specific procedures or supervises the performance of specific procedures to meet protocol requirements (e.g., EKG, treadmill, phlebotomy, and hospital procedures).brMaintains current, accurate flow sheets, case reports, data bases, and study logs (e.g., screening, enrollment, and drug dispensing/drug return logs).brDocuments and communicates adverse events per research protocols and regulatory standards./li /ul brbKnowledge, Skills, and Abilities/bulliKnowledge of medical terminology and clinical research requirements./li/ulbrpSharp HealthCare is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability or any other protected class/pbr