- Lilly (Indianapolis, IN)
- …the trial sponsor in recent years. The role of the Clinical Trial Label Regulatory Compliance Associate is to participate in maintenance and ... interpretation of the clinical trial (CT) material label ...product. To accomplish this, it is necessary for the Associate to develop collegial and mutually productive relationships across… more
- ThermoFisher Scientific (Greenville, NC)
- …and supports business development activities. Provides medical review and analysis for clinical trial serious adverse events, marketed products ICSR and periodic ... modules, etc. to ensure that the medical content is accurate and complete. ** Clinical Trial Support:** + Monitors all safety variables (AE, laboratory… more
- Catalent Pharma Solutions (Philadelphia, PA)
- …**The Role** + Monitors, organizes and performs all functions associated with packaging of clinical trial supplies and assures compliance to GMPs, SOPs, FDA, DEA ... one year of Clinical , contract or production experience required + Clinical Trial Manufacturing and Packaging experience preferred + Computer literate… more
- Catalent Pharma Solutions (San Diego, CA)
- …records, packaging, labeling, assembly, supply chain, procurement and distribution of clinical trial materials, pharmaceutical/biotech environment is preferred + ... ** Associate Project Lead, Pre-production** **( Clinical Supply)**...activities related to supply chain, procurement, batch record and label creation, and other project management and coordination activities… more
- Catalent Pharma Solutions (Kansas City, MO)
- …stand-alone and integrated biologics projects._ The Kansas City **Supply Chain Distribution Associate II** supports clinical trial projects through ... **Distribution Associate II** **Position Summary:** + **Work Schedule:** M-F...Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. The site provides a range… more
- AbbVie (Mettawa, IL)
- …research delivery. + Utilize HEOR expertise and payer/HTA insights to shape clinical trial measurement strategies and interface with global regulatory bodies ... LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Purpose: The Associate Director works independently with guidance from a Director and is… more
- Veterans Affairs, Veterans Health Administration (Sioux Falls, SD)
- …The incumbent is responsible for the quality assurance of images (positioning/ label /technique/network information) prior to transmission to the PACS network. The ... in the "Required Documents" section of this announcement. Completes and signs a trial period acknowledgement form which outlines the conditions of the 1 or 2… more
- Veterans Affairs, Veterans Health Administration (Columbia, SC)
- …Uses two identifiers to Identify patients before starting any Radiology exam/procedure. Properly label all images with Right or Left markers. This is essential so ... position, you will be required to serve a 2-year trial period during which we will evaluate your fitness...the incumbent [can operate independently] and has demonstrated specific clinical competency in the appropriate specialty and taken and… more
- Veterans Affairs, Veterans Health Administration (Lincoln, NE)
- …their assigned tasks mostly independently. DRTs may have varying assignments including clinical instruction, basic QM type duties within the program, scheduling and ... departmental procedures. Responsible for the quality assurance of images (positions/ label /technique/network information) prior to transmission to the PACS network.… more
- Veterans Affairs, Veterans Health Administration (Miami, FL)
- …Be responsible for the quality assurance of the image such as positioning, label , technique, and net work information. Any deviance in technique which alters patient ... will be required to serve a 1 or 2-year trial period during which we will evaluate your fitness...radiologic technology program, evidenced by a certificate or an associate degree, accredited by the Joint Review Committee on… more
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