Oncology Clinical Research Nurse Coordinator

7 days ago

New Brunswick, United States Actalent Full time

Job Title: Oncology Clinical Research NurseJob DescriptionThe primary purpose of the Clinical Research Nurse (CRN) is to ensure the successful, patient-oriented, safe, and effective conduct of clinical trials. The CRN assists investigators in preparing and implementing new clinical trials, screens and enrolls study participants, and provides protocol-related clinical management to those participants while on study. The CRN serves as a resource to other faculty and staff on available protocols and general research topics such as FDA, IRB, and GCP regulations.ResponsibilitiesCollaborate with the Protocol Activation office to initiate and activate new clinical trial protocols.Prepare and review study tools such as study binders, medication diaries, eligibility checklists, and flow sheets.Verify Scientific Review Board (SRB), Institutional Review Board (IRB), data collection plans, and finance/contract approvals prior to study activation.Review protocols and collect multidisciplinary feedback to identify and resolve potential obstacles to safe, effective study conduct.Perform one-on-one or group protocol-related nursing education to facilitate safe, effective care of enrolled patients.Translate finalized protocol treatment plans, study calendars, and clinical trials billing grids into sample orders.Collaborate with the clinical research team to ensure timely pre-screening of potential subjects and active cancer patients for available clinical trials.Review patient charts and medical history to confirm protocol eligibility and obtain necessary source documents.Follow the required elements of the informed consent process to ensure IRB-approved informed consent has been obtained.Provide backup support to register consented research patients with study sponsors and input data into the clinical trials database.Serve as a resource for Clinical Trial Billing Information related to assigned studies.Act as an essential link between patients and other members of the research team.Identify, address, and communicate challenges with protocol procedures and timelines to the study team and supervisor.Ensure protocol-specific orders are executed accurately, including scheduling and completion of tests and appointments.Coordinate protocol-specified procedures and treatments between disciplines and sites of care.Manage patient reimbursement while on clinical trial.Deliver high-quality, compassionate oncology nursing care in coordination with the assigned clinical team, investigators, and ancillary departments.Provide nursing assessment of study patients and ensure complete and accurate nursing documentation for protocol-specified visits.Collaborate with all integrated medical system staff to ensure timely delivery of services to patients.Qualifications: Graduate of an accredited school of nursing with a license to practice in the State of New Jersey.Bachelor's Degree in Nursing.Two years of oncology nursing experience required.One year of clinical research experience Oncology Nursing Society (ONS) certification as an Oncology Certified Nurse (OCN) or Advanced Oncology Certified Nurse (AOCN) preferred.Proficient in computer applications (Word, Excel, etc.).Excellent communication and interpersonal skills.About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: Hiring diverse talent Maintaining an inclusive environment through persistent self-reflection Building a culture of care, engagement, and recognition with clear outcomes Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

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