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Cross-Functional and Global Collaboration: Partner across US and Global Medical, Commercial, Clinical Development, Regulatory, Market Access, Pharmacovigilance, Statistics, Translational Research, Manufacturing and Quality, Project Leadership, and Field Medical to align priorities and advance the US lymphoma medical strategy. Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays.

YEAR

Bristol-Myers Squibb Co

Senior Director, US Medical Affairs, Lymphoma

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Precision's uniquely integrated offerings enable the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for complex disease states. Essential functions of the job include but are not limited to: Oversees all aspects of study site management to ensure patient safety is protected, quality of data generated by managed sites resulting in consistently low query levels and in acceptable Quality Assurance reports.

Precision Medicine Group LLC

Clinical Research Associate II - FSP

FULL_TIME

OTHER

Human Subjects Research As applicable, oversee the submission of necessary documents required by the NYU Institutional Board (IRB), NYU Office of Clinical Trials and any other appropriate parties in order to obtain approval to conduct human subjects research (e.g., ensures the update and submission of necessary documents and/or forms to appropriate destination). This may include abstraction of data from the patient chart (e.g., laboratory or diagnostic test results, surgical/radiation treatments delivered, adverse drug reactions, etc); abstraction of data for publications, or data collection from outside physicians offices.

NYU Langone Health

Research Coordinator

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Human Subjects Research : As applicable oversee the submission of necessary documents required by the NYU Grossman Institutional Board (IRB), NYU Office of Clinical Trials and any other appropriate parties in order to obtain approval to conduct human subjects research (e.g., ensures the update and submission of necessary documents and/or forms to appropriate destination). Reviews all the elements of the screening process with the Principal Investigator that being: inclusion/exclusion criteria, completed informed consent, documentation of the event and the patient/subject willingness to participate in the study, Financial Development : Develops a draft and final budgets in conjunction with budget specialist assigned to the Transplant Institute for submission to the Supervisor/Principal Investigator.

Security Investigator Jobs in New York, NY

Senior Director, US Medical Affairs, Lymphoma Bristol-Myers Squibb Co

Clinical Research Associate II - FSP Precision Medicine Group LLC

Research Coordinator NYU Langone Health

Senior Research Coordinator NYU Langone Health

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