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Oncology Clinic Research Nurse

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Nashville, TN

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Description is theresearch arm of HCAu2019s global cancer enterprise. Focused on advancing therapiesfor patients, it is one of the worldu2019s leading clinical research organizationsconducting community-based clinical trials in oncology, cardiology andorthopedics through affiliations with a network of more than 1,000 physiciansacross the United States and United Kingdom.u00a0 We believe our success is dependent on a healthywork environment where staff members are the core of advancing therapies forpatients and accelerating drug development. We apply the same compassion andcommitment we have for our patients to our co-workers and colleagues andpromote an entrepreneurial culture.u00a0 Summary of Key Responsibilities: Primary responsibility is to screen, enroll and follow study subjects ensuring protocol compliance and close monitoring while the subjects are on study. Duties and Responsibilities: Duties include but are not limited to: Supports enrolling patients onto clinical trials through recruitment, screening, enrollment andfollow up of eligible subjects according to protocol requirementsu00a0 Ensures the protection of study patients by timely adherence to protocolrequirements/complianceu00a0 Uses the protocol as the only tool to screen, treat, and follow patientsu00a0 Reviews the study design and inclusion/exclusion criteria with physician and patientu00a0 Completes and documents screening/eligibility accuratelyu00a0 Completes and documents the informed consent process accurately and have all parties fullyexecute the document including HIPAA Authorizationu00a0 Completes the inclusion/exclusion form and standard enrollment form accuratelyu00a0 Accurately completes and submits the on-study forms within two weeks of enrollment forinvestigator-initiated protocolsu00a0 Ensures that patient documentation is completed at each clinic visit while in screeningu00a0 Ensures that all medications are approved by the registrar prior to initiating treatment or whenchanging medication regimens, such as crossover studiesu00a0 Accurately calculates and documents the BSA, creatinine clearance, urine protein:creatinineratio or any other conversions needed per protocolu00a0 Ensures that follow-up appointments, scans, or any related procedures are scheduled correctlyaccording to protocol requirementsu00a0 Informs and documents appropriate SCRI and clinic personnel when patient comes off studyu00a0 Re-consents patients at the next scheduled visit and documents process appropriatelyu00a0 Attends monthly staff meetings, if required and participates in start up training for new studiesu00a0 Maintains patient confidentiality according to ethical and legal requirements Mandatory: u00a0 Practices and adheres to the u201cCode of Conductu201d philosophy and u201cMission and Value Statementu201du00a0 During your employment with SCRI you will be routinely assigned training requirements. Youare expected to complete any training assignments by the due date. Qualifications Competencies: Knowledge:u00a0A body of information needed to perform tasks; May be obtained through education,training or experienceu00a0 Working knowledge of medical and oncology research terminologyu00a0 Abilities:An underlying, enduring trait useful for performing duties Ability to communicate and work effectively with a diverse team of professionals. Ability to work with minimal supervision at offsite facilities. Education: Minimum Required: Associate's Degree (2 yr program) Preferred: Bachelor's College Degree (4 yr program) Experience: Oncology nursing experience Clinical research experience Certification/License: Current RN license to practice in the state of Tennessee Current BLS certification :

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