Overview
Responsible for supporting the management and coordination of tasks for multiple clinical research studies to include screening patients for eligibility and participates in the subject's study visits and required activities per protocol. Duties include but not limited to assuring protocol compliance for all patients enrolled in the trial, participation in the informed consent process, perform ongoing assessments and documentation in collaboration with physicians and other providers, and participation in required training and education, Assures site research quality by practicing in compliance with US Oncology Research, Inc. (USOR) Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations through OSHA, CDC and HIPPA. Supports and adheres to US Oncology Compliance Program, to include the Code of Ethics Business Standards....Your Role At Voxeet This is your chance to use your technical and business acumen to advise and guide our customers. As our Customer Success Specialist, you will build and grow relationships with customers from the proof-of-concept stage all the way to go live....
...address unmet medical needs and improve life by advancing the care of patients with life-threatening diseases.Senior IT Business Systems Analyst - G&AGilead IT is looking for a Senior Business Systems Analyst to support the General & Administration organizations. The...
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...1354BR Requisition ID 41354BR Business Unit COR Job Description CDM Smith is seeking a DevOps Cloud Architect to join our Digital Engineering Solutions team. This individual will be part of the Development group within the Digital Engineering Solutions...