- Sonora Quest Laboratories (Tucson, AZ)
- …and reviewing SOPs. Assumes Clinical Consultant responsibilities and participates on site and system-level committees as assigned/required. This position will hold a ... faculty appointment with the University of Arizona Department of Pathology. Performs all functions according to established policies, procedures, regulatory and accreditation requirements, as well as applicable professional standards. MINIMUM QUALIFICATIONS… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …and complaint product supply.Key Responsibilities Support compliance activities for site Quality Operations in accordance with Legend standards, procedures and ... cGMPs.Collaborate with site personnel to provide guidance and determine resolution for manufacturing issues.Ensure accurate and timely maintenance and review of… more
- Legend Biotech USA, Inc. (Atlanta, GA)
- …Biotech sponsored clinical trial sites to include, but not limited to, site identification, patient accrual discussions, site initiation or feasibility and ... to serve and the primary field-based point of contact between investigators and members of the Legend Biotech Medical Affairs and Clinical Development teams; Addressing AE management and education as needed.Collaboration with cross-functional partners… more
- AvalonBay Communities (Arlington, VA)
- …ensuring all work meets project specifications. Planning and Scheduling Develop comprehensive site plans addressing public safety, site security, logistics, and ... with key milestones and deadlines. Coordinate subcontractors, owners, and site contractors to ensure alignment with project requirements. Relationship Management… more
- United Site Services (Gastonia, NC)
- **About USS** United Site Services is the industry leader in comprehensive site services, committed to creating partnerships that help enable our customers' ... and reliable experience for our customers. By joining United Site Services, you will be part of an organization...and install fence panels, with appropriate tools, at work site in accordance with pre-determined specifications. Locate, measure and… more
- ASRC Industrial Services (Tempe, AZ)
- …Federal compensation programs, the Department of Energy Office of Legacy Management (LM), site operations project and technical leads, and to other areas across the ... and providing research for Federal compensation programs, DOE LM managers, LMS site and project leads, and other operations and support organizations within LMS… more
- Parexel (Raleigh, NC)
- The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator ... Practices (GCP), and the Sponsor's standards. The Sr. CRA is accountable for site management and monitoring, managing investigator site relationships to ensure… more
- Parexel (Little Rock, AR)
- …and efficient manner. The CRA acts as the main contact with the study site and has the responsibility for monitoring the study conduct to ensure proper delivery ... their respective commitment in the individual studies. **Key Accountabilities** : ** Site Management Responsibilities** + Contributes to the selection of potential… more
- VitalCore Health Strategies (Hopkinton, MA)
- …care in a region. Serve as liaison for clinical matters related to on- site , off- site specialty care, emergency department services, and inpatient care. Provide ... 24/7 on call back up for site Medical Directors. Participate in Continuous Quality and Safety...functions, including clinical quality indicators, patient safety chart and site audits. Adherence to Utilization Management (UM) programs specific… more
- Parexel (Boston, MA)
- …Purpose:** The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials ... and sponsor standards. The Sr. CRA is accountable for site management and monitoring, managing investigator site ...for site management and monitoring, managing investigator site relationships to ensure effective delivery of clinical trials… more
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