229 cloud-computing-"https:"-"https:"-"https:"-"https:"-"https:"-"UCL" positions at University of Oklahoma
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eligible to participate in a clinical trial or research program, distributes information, acts as a clinical resource, manages data, conducts follow-up care for patients, and attends meetings pertaining
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, and maintain the departmental training program, including specialty equipment training to ensure compliance with safety standards. Assist in creating, modifying, and training on departmental SOPs and
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job opportunity that could be right for you! The Clinical Trials Manager – Regulatory Affairs provides senior administrative management to the clinical trials program by overseeing, training and
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environment. Communicate effectively. Engage in repetitive motion. Use of computer and calculator. Equal Employment Opportunity Statement The University, in compliance with all applicable federal and state laws
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Working Conditions: Physical: Sitting for prolonged periods. Communicate effectively and listens. Engage in repetitive motion. Use of computer and telephone. Environmental: Standard Office Environment
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Clinical Trials Office here. Duties: Identifies, recruits, and schedules patients who may be eligible to participate in the oncology clinical research program. Performs the initial assessment of potential
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, Neuroscience, Biochemistry, or Microbiology with a computational focus; Computer Science with a biological focus; or a related discipline) Skills: Knowledge of cell, molecular biology, and bioinformatics
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, program evaluation, data collection, or support roles in academic or community-based research settings. Knowledge, Skills, & Abilities: Clear and professional written and verbal communication, including
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*Research Coordinator - HPRC - Job Number: 260402 Organization : Stephenson Cancer Center Job Location : Oklahoma-Oklahoma City-Health Sciences Center Schedule : Full-time Work Schedule: Monday-Friday 8am-5pm Work Type: Onsite Salary Range: Targeted annual salary ranges from $38,700 to $50,300,...
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procedures. Enters data and maintains on-going compliance with NCI Clinical Trial Reporting Program requirements. Coordinates schedules, formulates agendas and takes minutes for all PRMS related meetings