- University of Rochester (Rochester, NY)
- …and approval of case report forms (CRFs) and study-specific procedure manuals and documents. Clinical trials coordinator II for the University of Rochester ... in clinical trials . + Conduct FDA-registration quality clinical trial visits, including, consenting, visit assessments, intervention distribution, and… more
- University of Utah (Salt Lake City, UT)
- …The research assistant/analyst will work closely with the principal investigator, research coordinator , clinical staff, and regulatory entities to ensure ... to vaccinations. **Preferences** Prefer a candidate with prior experience with clinical trials , research assessments, and brain stimulation. **Type** Benefited… more
- University of Washington (Seattle, WA)
- …The purpose of this position is to support the research objectives of the Clinical Trial Unit. Division of Cardiology physicians address the prevention and ... into best practices and improvement of patient care. The Clinical Trials Unit (CTU) at the University...of the research projects. Research Study Assistants with the Clinical Trial Unit provide assistance and support… more
- Veterans Affairs, Veterans Health Administration (Cleveland, OH)
- …limited to the following: Maintains and demonstrates knowledge of professional clinical laboratory science principles, practices, concepts, and theories that support ... results recorded into the computer system. Performs checks to maintain compliance with regulatory bodies such as AABB, FDA, The Joint Commission (TJC), College of… more
- Novant Health (Mount Airy, NC)
- …such as Microsoft Office (Word, Excel, Outlook). + Experience working with databases or clinical trial management systems is highly desirable. What We Offer: + ... Institute in Mount Airy, NC. This is not a Clinical Research Coordinator Position. The Specialist supports... Clinical Research Professionals (ACRP), the Society of Clinical Research Associates (SOCRA), Regulatory Affairs Professionals… more
- Veterans Affairs, Veterans Health Administration (Mather, CA)
- Summary The Clinical Laboratory Scientist is responsible for evaluating, performing, interpreting, and validating the accuracy and validity of test results. ... Demonstrates a clear progression of clinical knowledge and experience by performing testing procedures on...spoken English. You may be required to serve a trial period. Subject to background/security investigation. Selected applicants will… more
- Veterans Affairs, Veterans Health Administration (Fresno, CA)
- …KSAs: Ability to communicate orally and in writing to persuade and influence clinical and management decisions. Expert understanding of regulatory and quality ... Summary The Clinical Pharmacy Specialist (CPS) at VA Central California...ineligible to apply for incentive. Contact ###@va.gov, the EDRP Coordinator for questions/assistance. Learn more Permanent Change of Station… more
- Veterans Affairs, Veterans Health Administration (Orlando, FL)
- …and influence clinical and management decisions. b. Expert understanding of regulatory and quality standards for their program area. c. Ability to solve ... EDRP participants ineligible to apply. Responsibilities The primary responsibility of the Clinical Pharmacy Specialist (CPS) in mental health is the provision of… more
- Actalent (New Brunswick, NJ)
- …a Clinical Research Coordinator (CRC). + Strong understanding of clinical operations and regulatory compliance. + Bachelor's Degree in a science ... a dedicated and experienced Research Study Manager to oversee the day-to-day clinical research operations. This role requires a proactive leader with strong… more
- University of Colorado (Aurora, CO)
- …**Job Summary:** **Key Responsibilities:** + Oversee the day-to-day operations of clinical trials , mixed-methods studies, and community engagement activities, ... experience with management of multiple research studies including randomized controlled clinical trials , mixed methods research, and qualitative research, which… more