Clinical Research Coordinator II (CRC2) Tucson

Clinical Research Coordinator II (CRC2) TucsonArizona Liver Health (ALH) is dedicated to driving high standards of care and advancing medical innovation through leading clinical trials, ensuring patient safety and regulatory compliance, and generating high-quality clinical data. Our network of multiphase, multitherapeutic research, standard of care, and VEN Centers sites is staffed by skilled providers, research, clinic, pharmacy, and patient outreach professionals. ALH operates state-of-the-art facilities and programs to meet the evolving needs of clinical research and overall patient treatment.Arizona Liver Health/Arizona Clinical Trials is looking for qualified candidates for the Clinical Research Coordinator II position in Tucson, AZ.Title: Clinical Research Coordinator II (CRC2)Compensation: $27.50 to $33.00 per hour, depending on experienceStatus: Full-time, Non-exemptLocation: Tucson, AZSchedule: Monday-Friday, 7am-4pmEssential job functions/duties:Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.Under the direction of the Principal Investigator or sub-investigator, manage the conduct of clinical research activities.Responsible for coordinating and implementing assigned protocols in compliance with FDA CFR, GCP and company SOPs.Collects and records clinical research data, assists in patient assessments, scheduling, maintain study files, study supplies and study medication accountability.Develop management systems and prepare for study initiationReview with the Principal Investigator the inclusion/exclusion criteria, overall structure and requirements of each protocolReview the protocol summary sheet and the Informed Consent Form for accuracy and clarity about these protocols to staff and patients.Responsible for the recruitment and screening of potential participants, which includes chart review of patients and schedules, contacting leads from outside recruitment efforts, and following up on referrals from all sources.Responsible for meeting recruitment goals for each study.May assume primary responsibility in the implementation and management of new clinical trials in a knowledgeable and collaborative manner.Performs all functions according to established policies (SOPS), procedures, regulatory and accreditation requirements, as well as applicable professional standards.Provides educational information to subjects. Serves as a resource and support person for subjects and families by being a consistent person they can contact within the clinical research program.Provides all employees and research subjects with an excellent service experience by consistently demonstrating professional decorum.Serves as a liaison to all physicians, employees, and third-party vendors.Record data and study documentationKeep the clinical trial management system updated with newly recruited subjects, tracking completed visits and stipends for the participants and investigators and ensuring status of each patient is accurate.Assign patient stipend pay card at screeningDocument reason for screen-fail in real timePlans, prepares and performs tasks required by protocol, which may include, but not limited to the following:Record data as directed using the appropriate media or platformFollow procedures for access and security for electronic data entryReview keyed data for accuracy as neededSend data to the data collection center on a timely basisMaintain source documentation for all data entered, including clinic chart visit notes, lab data and procedure reportsDevelop and/or edit source as needed independently or with Quality Assurance / Quality Control team to ensure compliance with protocol and EDC.Correct and edit data as directed and as appropriate.Informed ConsentObtaining patient medical history and medication listsPhlebotomy and basic laboratory testsProcessing & shipping labs for central and local labsPatient education and trainingECGAdminister questionnaires and assessmentsVital signsCollect information for adverse event reportingAssist with efficacy assessmentsData Entry and Query ResolutionStudy drug administration, including injectionsTracking study supply inventory and reordering when necessarySchedule patient visits in appropriate electronic systemsDocumenting all patient visits and communications in progress notesDocument and record all AEs and SAEs as outlined in protocolMonitor and report adverse eventsTriages adverse events and communicates with the research physician regarding the occurrence of adverse and serious adverse events within 24 hrs. Follow-up with the subject and collaborate information as needed.Responsible for administrative duties including filing documents related to subject's participation in research, regulatory, lab results, receipts, invoices, calibration reports, etc.Ensure W-9 and medical release forms are signed by subjects annually.Management of site activities during audits and inspectionsManagement of ancillary staff as assignedTrain and supervise support staff (e.g., CRC I)Mentor for externsTrain newly hired employees as either Research Assistant and/or CRCPrepare for quality assurance audits and regulatory inspections as neededAct as contact person before, during and after audits and inspectionsProvide all required documentation to auditorsMake all appropriate corrections as requested by auditorsCoordinate site response to audit/inspection findings.Participates in monitoring visits from sponsor provided appointees, ensures monitors are able to meet/speak with PI and ensures all concerns are addressed in a timely manner.Other responsibilities as delegated by manager.Knowledge/Skills/Abilities required:Minimum (2) years of experience working previously as a Clinical Research Coordinator for late phase clinical trials.Experience and training in the conduct of clinical research (specific experience and/or training in clinical research, including IRB submissions, reporting and source documentation, trial management).A thorough understanding of regulatory requirements, principles of GCP and biomedical research ethics.Interpersonal and communication skills—interact effectively with professional, administrative staff, sponsor and regulatory representatives, patients, potential subjects and referral sources.Possess a sound and in-depth understanding of each protocol that has been assigned as a primary responsibility protocol deviations, serious adverse events and other reporting requirements.Able to perform all Job duties listed for Job Description for PhlebotomistKnow and understand all regulatory requirements associated with the conduct of the study assigned.Travel requirements:Some interoffice travel may be required with use of company vehicle or mileage reimbursementEducation, credentials, and/or trainings required:Associates or Bachelor's degree in healthcare, clinical research management, or related required.Master's degree or study-specific training preferredGCP certification required at hire.Experience and training in the conduct of clinical research and basic knowledge of medical terminology.Experience and training in the conduct of clinical research (specific experience and/or training in clinical research recruitment, including IRB submissions and trial enrollment management)Experience with data management and tracking softwareBenefits & Perks:Health, Dental, Vision (with HSA plans and employer contribution)3 weeks of PTO5 days Sick Time401K with 6% company matchShort & Long Term DisabilityCEUs / Educational AssistanceShared company vehicles for required travelEEO statementIt is the policy of the Institute for Liver Health DBA Arizona Liver Health and Arizona Clinical Trials to provide equal employment opportunities without regard to race, color, religion, sex, national origin, age, disability, marital