- University of Miami (Miami, FL)
- …organizations including but not limited to Oncology Nursing Society's Manual for Clinical Trials Nursing. + Participates in the development and revision ... + Ensures compliance with all facility policies and procedures and all regulatory and governing body standards and regulations. Staff Development: + Provides… more
- Pfizer (Groton, CT)
- …you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials , you will apply cutting edge design and process development ... leading by example, showing mastery of all animal handling SOP's, regulatory guidelines and Pfizer policies. + Exemplify work-place standards, positive habits… more
- Veterans Affairs, Veterans Health Administration (Northport, NY)
- …budget execution. Responsible for maintaining adequate staffing by GS-11 Clinical Laboratory Scientists in the Chemistry, Hematology, Coagulation and Urinalysis, ... competency assessment of assigned staff. Works together with other clinical and administrative service chiefs and program managers to...will be required to serve a 1 or 2-year trial period during which we will evaluate your fitness… more
- ProMedica Health System (Toledo, OH)
- …helpful, but an understanding of federal and state regulations relating to clinical trials contracting (eg subject injury and indemnification, intellectual ... parties. + Develops and maintains a centralized tracking system for all clinical research contracts, providing regular metrics and status updates on negotiations and… more
- AnMed Health (Anderson, SC)
- …This person also has direct responsibility for buying functions for specified clinical as well as non- clinical areas and professional services departments. ... conversions, and contract implementations as necessary. * Manages contracts for their clinical areas to ensure suppliers and distributers are compliant with agreed… more
- Veterans Affairs, Veterans Health Administration (Cleveland, OH)
- …Health Professional The incumbent serves as the Assistant Laboratory Manager for Clinical Pathology in the Pathology and Laboratory Medicine Service (PALMS) at Louis ... decisions of other experts in almost all areas of clinical medicine and has direct impact on the wellbeing...will be required to serve a 1 or 2-year trial period during which we will evaluate your fitness… more
- Bristol Myers Squibb (Summit, NJ)
- …and unique perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of passion, innovation, urgency, ... current Good Manufacturing Procedures (cGMP), USP, EU and other global regulatory requirements. + Drive completion, adherence to training requirements and assess… more
- Veterans Affairs, Veterans Health Administration (Cleveland, OH)
- …Rewards of a Allied Health Professional he incumbent serves as a Supervisory Clinical Laboratory Scientist (CLS) on the Esoteric, Send-Out Testing and Phlebotomy and ... and state laws and regulations and laboratory accrediting agency regulatory requirements sufficient to develop plans and procedures for...will be required to serve a 1 or 2-year trial period during which we will evaluate your fitness… more
- Bristol Myers Squibb (Summit, NJ)
- …and unique perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of passion, innovation, urgency, ... a controlled, cGMP cleanroom environment. Lead Manufacturing Associate adheres to regulatory requirements while performing job functions. Job duties are performed… more
- Veterans Affairs, Veterans Health Administration (Bay Pines, FL)
- …duties and responsibilities are carried throughout the Healthcare Center including all clinical and other patient care areas involved with the services. Duties and ... Not Authorized Total Rewards of a Allied Health Professional Clinical Laboratory Scientist: vacareers.va.gov/wp-content/uploads/sites/5/Total-Rewards-of-a-Medical-Technologist-Career-Flyer.pdf Requirements Conditions of Employment You… more