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 Coordinator (CRC) is a professional working under the direction of their Novant Health leader in conjunction with study investigators.. Clinical Research Coordinator I RN. Clinical Research Coordinator II RN. Clinical Research Coordinator III RN. Clinical Research Coordinator IV RN
Join us and discover why Modern Healthcare Magazine named us in its Top 100 Places to Work. Overview: 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. Performs duties and responsibilities in a manner consistent with our mission, values, and Mercy Service Standards.
Under the direction of the Cancer Research Manager, the Cancer Center Medical Director and other participating physicians conducts all protocol specific research activities including but not limited to recruitment, assessment/consent process, treatment, patient care (standard and protocol-related), data collection/CRF completion, participating in monitoring visits, responding to monitoring/audit reports, and conduct of patient follow-up in conjunction with Investigators. The Sisters of Providence and Sisters of St. Joseph of Orange have deep roots in California, bringing health care and education to communities from the redwood forests to the beach shores of Orange county - and everywhere in between. In Southern California, Providence provides care throughout Los Angeles County, Orange County, High Desert and beyond. Our not-for-profit network provides a full spectrum of care with leading-edge diagnostics and treatment, outpatient health centers, physician groups and clinics, numerous outreach programs, and hospice and home care, and even our own Providence High School. Category:Healthcare, Keywords:Research Nurse, Location:Garden Grove, C92840
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.
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
Prime Staffing is seeking a travel nurse RN Research / Clinical Research for a travel nursing job in Denver, Colorado.. Responsibilities include health education, chronic disease management, medication administration, and supporting procedures.. Onboarding may take 2–4 weeks depending on document submission and clearances.. We offer a wide range of staffing services including temporary, temp-to-perm, and direct hire placements.. Our extensive network of qualified candidates includes nurses, allied healthcare professionals, corporate support professionals and executives.
The Nursing Quality and Regulatory Compliance Manager is responsible for enhancing the clinical quality and outcomes of Nursing practice using clinical data and project planning, implementation, and evaluation by applying evidenced-based best practices throughout Sinai Chicago.. The Nursing Quality and Regulatory Compliance Manager has the specific responsibility for providing leadership and direction in overall Nursing quality and regulatory compliance.. Experience in EPIC and MEDITECH software systems preferred.. Along with Employer Paid Life and Accidental Death & Dismemberment (AD&D), Supplemental Life, Short-Term and Long-Term Disability, Health Savings Account (HSA) and Flexible Spending Account (FSA), Employee Assistance Program and Student Loan Assistance.. Registry Caregivers are not eligible for Sinai's benefit programs with the exception for Sick-C, PPO Medical Plan, Employee Assistance Program (EAP) and non-match eligible contribution to the Sinai Health System Consolidated 403(b) retirement savings plan.
Job is at a clinical research facility.. Preparing for upcoming studies, service healthy population of patients during clinical trial studies, dosing, watching for side effects to trials, administering trial doses, reporting and investigating side effects. This would be the perfect fit for those looking to transition from hospital settings into nursing lab settings. Working with only healthy population of candidates during medical dosing trials. Must be proficient with computers and electronic charting as Nurses are required to document trial doses and effects into computer systems
We are currently seeking a Clinical Research Nurse, to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment.. If you join us, you will work with some of the world's leading pharmaceutical, biotechnology, and medical device companies in a vital stage of clinical development: establishing the safety, tolerability and pharmacokinetics of a new drug.. Ensure that the dignity, health, safety, and welfare of participants is given the highest priority at all times. Obtain Informed Consent and continue the ICF process by educating, explaining and informing participants of study procedures. Perform study related activities such as cannulation, telemetry, holters, vital signs, ECGs, venipuncture
As the preeminent institution in western Pennsylvania for the delivery of cancer care, the performance of basic, translational, and clinical research, and the education of the next generation of cancer researchers and physicians, UPMC Hillman Cancer Center is exceptionally well-positioned to contribute to the global effort to reduce the burden of cancer.. UPMC Hillman Cancer Center is currently hiring a regular full-time Clinical Research Nurse Coordinator (RN) to help support the Community Oncology Clinical Research Services (CRS) teams at our UPMC Hamot Oncology network office located in Erie, PA. This position offers a $6,000 sign-on bonus and will work a regular Monday through Friday daylight schedule with the Hamot Oncology network location.. This unique role allows for the clinical research nursing professional to work in the community and screen/enroll patients in all cancer disease centers with UPMC Hillman Cancer Center working as a Trials Coordinator.. The clinical research coordinator will work with physicians, nurses, other allied health professionals, and research staff to coordinate clinical research efforts provided at UPMC.. 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.
We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio.. The Clinical Research Nurse is a specialized research professional working with and under the direction of the clinical Principal Investigator (PI).. + Participate in nursing study related activities as required by protocol compliance with Corporate, divisional, and departmental SOP's and external (CFR, ICH GCP) regulatory guidelines.. + Interact with the Principal Investigator and other study physicians, Recruiting/Screening, Data Systems, and other personnel in support of study-specific activities.. + Nursing competency skills per scope of practice (i.e., performing vital signs, nursing assessments, performing ECG/EKG, administering injections, etc.)
Job Title: Research Nurse/Research Coordinator/Clinical Study Coordinator. The role of the study Research Nurse is to ensure patient safety and wellbeing.. The Research Nurse must be able to work independently, be a team player, and proactively problem solve.. Monitor and report adverse events: Assess, document and record all AEs as outlined in the protocolReport serious AEs o the Principal Investigator, Sponsor and IRB (and others as required by funding source or as outlined in the protocol).. Regulatory documentation:Know and understand all regulatory requirements associated with the conduct of the study assignedMaintain files and documents as regulations dictatePrepare and submit initial applications to central and local committees (IRBs, biosafety, radiology, etc.)
Under direct supervision of a physician and nurse (if applicable), is responsible for enlisting, maintaining, and assuring protocol compliance for all patients on clinical trials.. Collaborates with physician in determining eligibility of patients for clinical trials.. Ensures site research quality by practicing in compliance with Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations.. Provides a safe environment for patients, families, and clinical staff at all time through compliance with all federal, state, and professional regulatory standards as issued through OSHA and the CDC.. Interacts with the Clinical Trial Sponsors to recruit new clinical trials for the site.
Piper Companies is currently seeking a Clinical Research Nurse to support a reputable and growing hospital network in Philadelphia, PA.. Responsibilities of the Clinical Research Nurse. Qualifications of the Clinical Research Nurse. Compensation for the Clinical Research Nurse. Keywords: Clinical Research, RN, Nurse, CRN, Clinical Trials, Patient Safety, Patient Monitoring, IRB Submission, Sponsor Visit
Clinical Research Nurse Practitioner - Contract - San Antonio, TX. Are you looking to drive groundbreaking medical research and make a real impact-join our client and lead the way in advancing clinical trials!. Proclinical is seeking a Clinical Research Nurse Practitioner to join our client's team in San Antonio, TX.. The successful candidate will manage the daily operations of clinical trials, ensuring communication with investigators, sponsors, and study participants.. As a Nurse Practitioner, you will also perform medical assessments on patients as needed.
Clinical Research Nurse. Work collaboratively with physicians, Clinical Research Associates (CRA) and pharmacists to coordinate care for an assigned population of patients who are enrolled in to IRB clinical research trials.. Assess, identify and prioritize clinical information to physician, NP, PA and other clinicians for patients who are being evaluated or who are enrolled in to IRB clinical trials.. Assess and document signs and symptoms of illness, reactions to treatment, changes in physical or psychological condition and general appearance in accordance with the IRB protocol assuring that the documentation is complete and accurate in order to avoid protocol deviations.. Ensure the consent process is performed in compliance with institutional, FDA, IRB, clinical trial sponsor and other applicable regulations.
DelRicht is a clinical research company dedicated to providing an excellent customer experience to all patients that participate in our clinical trials. Our clinical trials provide new treatment options for our patients and ultimately our goal is to get new medications and medical devices FDA approved!. Clinical Research Nurse’s Main Objective: Overall, the Clinical Research Nurse is responsible for providing quality, excellent patient care and a great experience for our patients in our clinical research studies. Required: Registered Nurse (R.N.) or Licensed Practical Nurse (L.P.N).. This is an onsite Monday-Friday position traveling between Vienna, VA and Rockville, MD. No remote or hybrid-seeking applicants, please.
About the job Clinical Research Nurse. Nurses with experience in any of the following areas are strongly encouraged to apply: Clinical trial or study, Oncology, or Peer review.. Shift(s) available: day shift, night shift, and mid shift. Screen potential study participants and obtain informed consent prior to enrollment in research studies Administer study treatments, collect biological samples, and monitor participants throughout the study. Strong communication skills, both written and verbal, to effectively convey information to study participants, research staff, and stakeholders
Clinical Research Nurse I- Full Time Permanent (Thursday- Saturday Night Shift) 100% on site San Antonio TX. 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. Title: Clinical Research Nurse I. 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.