The Oncology Clinical Research Nurse (RN) of Cancer Clinical Research Office (CCRO) is an integral member of the research team.. Coordinate and facilitate the appropriate conduct of clinical research trials in oncology which may be supported by the NCI, industry, cooperative groups or HHC system alliances.. Coordinate and conduct the operation of clinical trials as per GCP and ICH guidelines including participant recruitment; informed consent; continuous monitoring of protocol for compliance and patient safety; source document review; data entry; sponsor monitoring.. Ability to work with spreadsheets (such as Excel), familiarity with databases (ex: Medidata, RAVE, IRIS, NSABP, GOG, RTOG etc.). Here, you are part of an organization on the cutting edge – helping to bring new technologies, breakthrough treatments and community education to countless men, women and children.
The clinical research nurse (RN) is a licensed professional caregiver who assumes responsibility and accountability for planning, delegating, and coordinating the direct research care of a group of patients during a designated time frame. The Research RN is responsible for assuring compliance with Federal and State regulations relating to research and the study protocol requirements. The RN coordinates and provides care through the therapeutic use of self, nursing process, and the environment and technology, in partnership and collaboration with interdisciplinary team members. 1 year Research Coordinator Preferred.. CCRC Certified Clinical Research Coordinator - ACRP Association of Clinical Research Professionals Preferred
The NICU Quality & Safety Nurse will lead patient safety and quality of care efforts while striving to create and maintain a culture of safety within the Newborn Intensive Care Unit (NICU).. Utilizing the principles of process improvement and change management, the NICU Quality & Safety Nurse will partner with department leaders to facilitate the implementation of evidence-based and regulatory standards of nursing and clinical practice, leading various large and small-scale quality improvement and health system projects with end-to-end ownership.. MSN or Masters degree in Healthcare or closely related field required within two (2) years of hire.. Certified Professional in Healthcare Quality (CPHQ) or Certified Professional in Patient Safety (CPPS) preferred.. Miscellaneous Benefits Pet Insurance, Legal Services, Vendor Discounts
The Clinical Research Nurse (CRN) is responsible for coordination of research studies conducted by Mercy Research. The Clinical Research Nurse is responsible for the day-to-day operational tasks related to clinical trials and performs a variety of duties including, but not limited to, volunteer recruitment, drug/device/supply inventory maintenance, interaction with physicians, nurses, office staff, patients, and clinical monitors. The Clinical Research Nurse will assist in training and preceptor duties. The study load and complexity will increase from the Associate Clinical Research Nurse responsibility, thereby increasing the overall number of enrollments and visits. The Clinical Research Nurse will assist with communication and relationship building with sponsors and CROs.
A Travel Clinical Research Nurse (RN) position is available for a 13-week assignment in Pahala, Hawaii, focusing on clinical research within healthcare settings. Genie Healthcare is seeking a travel nurse RN Research / Clinical Research for a travel nursing job in Pahala, Hawaii. Genie provides travel RN's flexibility, support, top pay scale, housing and the #1 rated, multi-state health insurance coverage. The management team has 20 years of experience in workforce solutions and staffing in medical and non-medical fields, roles ranging from Clerical job to Cardiologist to software developer to CEO. travel nurse, clinical research, registered nurse, RN travel assignment, healthcare, rotating shifts, medical insurance, travel nursing jobs, nurse staffing, patient care
Title: Clinical Research Nurse I - Neuroscience. Coordinates and implements research studies for assigned services under the direction of the Principal investigator in accordance with the standards of good clinical practice, federal and state regulations and institutional review board (IRB) requirements. Screening, study recruitment, preparation of IRB reports. Collecting source data for electronic data capture (EDC) systems or Case Report Form (CRF) completion. Preferred - CCRC (Clinical Research)
The Clinical Research Nurse, ensures that the health and safety of research participants and the integrity and quality of clinical trials, are maintained and conducted in accordance with federal, state, IRB, departmental, and institutional regulations, policies and procedures. The Clinical Research Nurse will primarily provide nursing expertise and care to research study patient management with primary focus on bone marrow transplantation and cellular therapy clinical trial protocols. They will serve as a liaison and work closely with investigators, department members, study sponsors, IRB and the institution, to support administration of compliance, financial, personnel and other related aspects of all ongoing clinical studies. Minimum 2 years experience in Pediatric Bone Marrow Transplant/Hematology-Oncology nursing required.. Knowledge of Institutional Review Board (IRB) policies and procedures
The Nurse Educator (Registered Nurse) is a vital member of the clinical team, responsible for integrating staff training and development with health information technology to improve patient care and health outcomes.. Current Commonwealth of Virginia Registered Nurse licensure, required. EMR configuration, technical support, and user education experience, required; API/ADT development/implementation experience, preferred. Advanced proficiency in all elements of needs assessment, instructional design and curricula development, clinical documentation and deliverables, systems analysis and design, software testing, training, adoption, and troubleshooting. Proficiency in organizational change management and proven ability to proactively identify and solve problems
The Patient Safety Specialist (RN) plans and facilitates programs to ensure compliance with patient safety standards and regulatory goals.. The Patient Safety Specialist (PSS) will be responsible for planning, organizing, and facilitating programs to ensure that all clinical departments are following the Joint Commission's National Patient Safety Goals (NPSG's) and MWHC's patient safety program.. The PSS will collect data through chart reviews and other methods while working with members of MWHC to identify opportunities to drive improvements in patient safety clinical outcomes and practice variation.. Assists with the identification of strategies to create and reinforce a culture of safety and continuous preparedness for NPSGs∯*∯ Collects clinical data and conducts chart reviews through utilization of the hospital medical record and information systems.. patient safety, clinical outcomes, risk management, root cause analysis, process improvement, chart review, nursing, healthcare compliance, medical record analysis, patient care quality
ensuring alignment with organizational objectives and regulatory requirements; and proactively anticipating future regulatory or industry changes, developing strategic plans to adapt policies accordingly. Guides evidence-based research and innovation by: identifying and exploring innovation opportunities in care delivery models and workflows; and contributing to a culture of innovation within the organization, encouraging experimentation and continuous improvement. Minimum two (2) years of experience in nursing informatics. Knowledge, Skills, and Abilities (KSAs): Systems Thinking; Health Care Data Analytics; Written Communication; Compliance Management; Stakeholder Management; Quality Improvement; Evidence-Based Medicine Principles; Nursing Principles; Business Acumen; Change Management; Health Care Compliance; Project Management; Strategic Alignment; Patient Safety; Clinical Quality Expertise.. TITLE: Clinical Informatics Nurse II
UPMC Hillman Cancer Center is currently hiring a regular full-time Clinical Research Nurse I (RN) to help support the Clinical Research Services team located at the Hillman Cancer Center in Shadyside/Pittsburgh, PA & at the UPMC Magee Women’s Oncology Research program in Oakland/Pittsburgh, PA. This role offers a $6,000 sign-on bonus and will support various Oncology Disease Center program studies working Monday through Friday daylight hours.. The Clinical Research Services (CRS) team is made up of nearly 200 staff members who facilitate the development, implementation, coordination, internal data monitoring, and completion of oncology-focused trials at Hillman.. Using a disease-specific centers model for conducting clinical trials, CRS provides study development and implementation assistance, submissions to the FDA, IRB processing, patient recruitment, study coordination, study-specific training, data collection, and specimen collection and processing.. The clinical research nurse will work with physicians, nurses, other allied health professionals, and research staff to coordinate clinical research efforts provided at UPMC. Facilitates compliance with the requirements of the research protocol and good clinical research practice while remaining cognizant of the needs of the diverse patient population.
The Clinical Research Nurse Coordinator promotes good clinical practices in the conduct of oncology clinical trials by possessing in-depth knowledge of federal regulations and guiding documents for the conduct of clinical trials and human participant protection.. In addition, the Clinical Research Nurse Coordinator assures compliance with protocol and regulatory requirements, manages patient protocol activities, assures patient safety, collects records and maintains data and source documentation.. The Clinical Research Nurse Coordinator performs all the duties and responsibilities associated with high-level, professional nursing practice including autonomous decision making based on predetermined protocol guidelines, nursing assessment and oncology knowledge.. Coordinates patient enrollment in clinical trial by following randomization procedures as per protocol, scheduling patient office visits, required screening assessments, ensuring appropriate specimen collection, batching and shipping per protocol and assessing participant compliance with the test article and follow-up visits.. Completes all required IT training to access to various Electronic Data Capture systems and Electronic Medical Records.
Here, you'll work alongside some of the best clinical talent in the nation leading the way in medical innovation and breakthrough research with Northwestern University Feinberg School of Medicine.. The Clinical Research Nurse reflects the mission, vision, and values of NM, adheres to the organization's Code of Ethics and Corporate Compliance Program, and complies with all relevant policies, procedures, guidelines and all other regulatory and accreditation standards.. The Clinical Research Nurse (CRN) is a registered professional nurse who demonstrates exemplary clinical research knowledge, has strong communication skills and is responsible for serving as a liaison between Northwestern University (NU) clinical research investigator teams (e.g., investigator-initiated trials, sponsor trials) and Northwestern Medical Group.. Sponsor or Sponsor representative(s) and IRB throughout the clinical trial.. Maintains research files, designs forms as needed, reports findings as appropriate, assists in preparation or review of material for submission to an IRB including reviewing and editing protocols and consent documents, where applicable.
The Nursing Informatics Specialist is a member of the Nursing and Epic Operations teams and is responsible to ensure clinical information system implementations are consistent with Dana-Farber Cancer Institute (DFCI) standards of nursing practice. Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. Current nursing licensure in the Commonwealth of Massachusetts. At Dana-Farber Cancer Institute, we work every day to create an innovative, caring, and inclusive environment where every patient, family, and staff member feels they belong. Dana-Farber Cancer Institute is an equal opportunity employer and affirms the right of every qualified applicant to receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other characteristics protected by law.
Under the direction of the Principal Investigator or designee, the Clinical Research Nurse I is responsible to carry out all delegated tasks related to complex protocols testing investigational drugs, devices, or research interventions.. The Clinical Research Nurse I is a a member of the team and resource for study protocol conduct acting as a liaison between the SLU SOM, clinical partners (ex.. SSM Health), the Principal Investigator, Institutional Review Board (IRB), and sponsors to ensure good clinical practice standards (GCP) throughout the life cycle of the study.. We currently have openers in Surgery, Nephrology, and the Cancer Center.. Maintains participant-level documentation for all studies, including those that are complex in nature, require access to the EHR or require SLUCare/SSM charge routing.
The Markey Cancer Center Precision Medicine Program is recruiting a Clinical Research Nurse II for several upcoming clinical trials.. This individual will coordinate cutting edge first in human clinical trials designed to advance Precision Medicine Cancer Care and associated clinical outcomes to all residents in the state of Kentucky.. In addition, the nurse researcher will serve as a resource to team members and other departments within the hospital as well as a liaison between investigators and study sponsors.. This position will have a fully on-site work arrangement.. ADN + 5 years of nursing experience required, or BSN + 3 years.
Clinical Research Nurse I- PRN/As Needed- Weekends 7AM-3 PM- ICON Salt Lake City UT. ICON plc is a world-leading healthcare intelligence and clinical research organization.. We are currently seeking a Clinical Research Nurse I to join our diverse and dynamic team.. As a Clinical Research Nurse I at ICON, you will play a pivotal role in supporting the execution of clinical trials, ensuring adherence to protocol requirements, and providing compassionate patient care throughout the research process.. + Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
The Clinical Research Nurse will join the Clinical Research Central Office (CRCO) at the University of Wisconsin Carbone Cancer Center (UWCCC) to coordinate cancer clinical research within one or more Disease-Oriented Teams.. The primary duties of this job involve the management of subjects enrolled in clinical research studies at the UW Carbone Cancer Center.. The University of Wisconsin (UW) Carbone Cancer Center has been an NCI-Designated Comprehensive Cancer Center since 1973.. UW Carbone is an integral part of the UW School of Medicine and Public Health and UW Health, bringing together more than 330 physicians and scientists from 50 departments and nine schools to conduct research and translate laboratory discoveries into new patient treatments.. UW-Madison will provide a paper copy upon request; please contact the University of Wisconsin Police Department.
The Nursing Research Specialist facilitates the development and implementation of research studies and evidence-based practice projects that transform pediatric nursing practice and improve patient outcomes.. The Nursing Research Specialist leads the development, implementation, and evaluation of innovative educational programs consistent with the guidelines for Nursing Professional Development.. Certified Research Specialist (CRS) - UAMS, Nursing Professional Development (NPD-BC) - American Nurses Credentialing Center. Participates in and incorporates research and evidence-based practice as a mentor, investigator, collaborator, translator, integrator and/or evaluator.. And we are nationally ranked by U.S. News & World Report ( for Cancer, Cardiology & Heart Surgery, Diabetes & Endocrinology, Nephrology, Neurology & Neurosurgery, Pulmonology & Lung Surgery and Urology.
HJF is seeking a Clinical Research Nurse who coordinates the activities associated with treating patients for clinical trials.. This position is the first of two Research Nurse levels.. The 59 MDW ST office advises and conducts clinical and translational research under the guidance of the Air Force Surgeon General (AF/SG), the Secretary of the Air Force (SAF), Air Force Chief of Staff, and the Office of Assistant Secretary of Defense for Health Affairs (ASD/HA) on matters pertaining to the medical aspects of the Air Expeditionary Force and the health of Air Force (AF) personnel and beneficiaries.. In order to support the required research, ST offices conduct translational research in the areas of emergency medical care, combat casualty care, force health protection, restorative medicine, clinical and rehabilitative medicine and specialty centers.. ST HQ continues to facilitate development of innovations for advancing the care and rehabilitation of the combat wounded and support for Food and Drug Administration (FDA) regulated trials supporting activities Enterprise-Wide. In order to support the required research, the ST HQ office requires support from a Technical Clinical Research Team (TCRT).