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The Oncology Research Nurse Practitioner I is an Adult Nurse Practitioner who manages the direct care of patients enrolled in clinical trials within the Herbert Irving Comprehensive Cancer Center at Columbia University Medical Center.
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At Ochsner, we participate in several multi-center clinical trials and have the support of an in-house Clinical Trials Unit and dedicated NICU research nurse. Experienced Neonatologists with training or experience as a principle investigator for clinical trials or recent graduates with experience in clinical trials are invited to consider joining our division working alongside a team of experienced neonatal nurse practitioners.
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Experience with outpatient reviews including DME, Genetic Testing, Clinical Trials, Oncology, and/or elective surgical cases preferred. The Utilization Management Nurse - Prior Authorization performs medical necessity reviews on prior authorization requests in accordance with national standards, contractual requirements, and a member’s benefit coverage while working remotely.
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As part of the LSU/LCMC network, the successful candidate will work in state-of-the-art facilities and engage in a robust clinical trials program. Engage in a vibrant clinical trials program offering patients innovative options.
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3+ years of experience with interacting with a wide range of suppliers (e.g., Contract Research Organizations, Cooperative groups, Clinical laboratories, Core laboratories including ECG and Imaging service providers): initiating, negotiating, and executing legal and/or financial agreements in the clinical trials environment- biotech or pharmaceutical industry.
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Execute on organization’s crop input market development plans by participating in customer field meetings, coordinated product trials, customer agronomy events, marketing support and delivery of crop planning services.
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Facilitate and coordinate daily activities related to clinical trials, playing a pivotal role in the study's execution. Requirements: Previous Clinical Research experience - Ideally 2+ Years of experience as a Clinical Research Coordinator; Ophthalmology/Retina Experience Preferred.
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Drafting Answers, Third-Party Demands, Cross Claims; propounding and responding to discovery, conducting and defending depositions (experts and lay witnesses), handling all aspects of motion practice, preparing Pre-Trial Orders, and preparing cases for mediations/arbitrations, judge and jury trials, and appeals are a daily part of the job.
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Summary Under the direction of the Executive Director of the Clinical TrialsOffice (CTO) or their designee, the Regulatory Coordinator independentlyperforms administrative and coordinative work directed toward the design,implementation, evaluation, and review of assigned Tulane Cancer Center (TCC)clinical trials by working closely with Principal Investigators (PI) and otherCTO staff members.
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Expert in regulatory affairs related to clinical trials research. Facilitate patient recruitment and enrollment into on-going clinical trials. Perform clinical trials duties in accordance with standards of nursing practice and the Code of Ethics and maintain awareness of what constitutes falsification of data or other research misconduct.
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Responsible for coordinating study enrollment, establishing a database/case load of patients, protocol treatment and follow-up care for patients participating in clinical trials. We are seeking a Clinical Program Manager (CPM) to join a team of investigators and advanced practitioners who are dedicated to delivering compassionate, expert, and comprehensive cancer care to patients and families who participate in clinical trials.
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Responsibilities:Take part in focus groups, clinical trials, online surveys/studies at home by following written and oral instructions. Work at Home - Part TimeAnyone looking for part-time, short-term work from home work is welcome to apply.
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Coordinates all aspects of clinical trials in accordance with the established protocols, FDA regulations, institutional policies, and ethical clinical practice. Ensures the efficacy of clinical trials by managing the documentation, safety procedures, and clinical interaction of patients, study sponsors, and physicians.
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The successful candidate will be responsible for performing blood draws during in-house clinicals, assisting in the design and execution of human subject trials, and conducting literature searches and reporting.
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Learn more about the company, our mission as well as see employee testimonies via our MRN website: Medical Research Network | Patient Centric Clinical Trials | MRN (themrn.io) We achieve our vision by conducting clinical trials directly in patient communities, reducing geographical, logistical, and socioeconomic barriers.
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trials job Company: Medix in Metairie, LA
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