RN - Clinical Research Nurse - Full Time - Days (UTICA, NY)

Job SummaryUnder the general direction of the Director of Clinical Research and the assigned Principal Investigator (PI) the Clinical Research Nurse (CRN) supports, facilitates, and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. The CRN works closely with the PI, designated department, sponsor, and institution (s), liaising and providing guidance on the administration of the compliance, financial, personnel and all related aspects of the clinical study. The CRN reports primarily to the Executive Director of Research Director of Clinical Research/Associated PI and interfaces with MVHS administration, compliance and Investigational Review Board.Core Job ResponsibilitiesFacilitate communication of study requirements to all individuals involved in the study. Provide appropriate training and tools for study team members. Documents date of training and signatures of study personnel trained on study specific training logAdhere to and educates stakeholders with/in the protocol specifics (study proceedings and timelines, inclusion and exclusion criteria, confidentiality, privacy, human protections)Collect documents needed to initiate the study and submit to the sponsor (e.g., FDA Forms 1572, CVs, etc.)Work with the PI to develop and implement recruitment strategies in accordance with IRB requirements and approvalsConduct or participate in the informed consent process including interactions with the IRB and discussions with research participants, including answering any questions related to the study. Obtain appropriate signatures and dates on forms in appropriate places. Assures that amended consent forms are appropriately implemented and signedScreen subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusionRegister participants in the appropriate coordinating center (if multi-site study) and in the billing matrix to ensure billing of study procedures to the appropriate funding sourceCoordinate participant tests and proceduresCollect data as required by the protocol. Assure timely completion of Case Report Forms Ensure adherence to study timelinesMaintain adequate inventory of study supplies. When handling investigational drugs/devices, follows the sponsor protocol and/or MVHS on Investigational Drug/Device AccountabilityComplete study documentation and maintain study files in accordance with sponsor requirements and organizational policies and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability formsRetain all study records in accordance with sponsor requirements and organizational policies and proceduresMaintain effective and ongoing communication with sponsor, research participants and PI during the course of the studyAssist PI in preparation of any modifications to the scientific protocol in accordance with federal regulations and university and sponsoring agency policies and proceduresWork with the PI to manage the day-to-day activities of the study including problem solving, communication and protocol managementEngage with subjects and understand their concernsPerform other duties as required. Education/Experience RequirementsREQUIRED:    Bachelor's Degree in Nursing/ Life or Health Science, or equivalent experience3 years of demonstrated sound theoretical and hand’s-on knowledge of the field of clinical research inclusive of planning, executing, and analyzing clinical research trials; performing protocol and site feasibility. clinical research experience in managing the various aspects of clinical trials at the sponsor, sponsor-designee, CRO, affiliate, vendor, and/or site level Skills: Excellent Communications Skills, Excellent Interpersonal Skills, General Clerical Skills, Microsoft Excel, Microsoft PowerPoint, Microsoft Publisher, Microsoft Word, Experienced with electronic IRB submissions, Clinical Trials Management Systems (e.g. CTMS) and Clinical Trials software platforms (Shared Investigator Platform WCG etc.)PREFERRED:Terminal degree in biomedical or educational sciences or equivalent experienceDiversified industry or investigator initiated clinical research experience demonstrating program and resource management across multiple projects, as well as proven leadership abilities Licensure/Certification RequirementsREQUIRED:    NYS RN LicenseDisclaimerQualified applicants will receive consideration for employment without regard to their age, race, religion, national origin, ethnicity, age, gender (including pregnancy, childbirth, et al), sexual orientation, gender identity or expression, protected veteran status, or disability.Successful candidates might be required to undergo a background verification with an external vendor. Job DetailsReq Id  97527 Department  RESEARCH AND SCHOLARLY ACT Shift DaysShift Hours Worked  8.50FTE 1 Work Schedule  SALARIED GENERALEmployee Status A1 - Full-Time Union Non-UnionPay Range $75k - $115k/Annually

Apply Now