- Wayne State University (Detroit, MI)
- Research Compliance Monitor , IRB Wayne...For-Cause Audits as requested by the Institutional Review Board Committee or Human Research ... compliance . Submit monitoring reports to the Human Research Protection Program Administration and to the Institutional...and protocol violations and direct to committee Chair, individual Institutional Review Board , institutional… more
- Wayne State University (Detroit, MI)
- …of essential regulatory documents and the execution of study protocol. Prepare IRB (Intitutional Research Board ) initial applications, amendments, ... occasionally accommodate participant schedules (mornings/evenings/weekends). Experience coordinating human subjects research or clinical trials. Familiarity with IRB … more
- University of Michigan (Ann Arbor, MI)
- …developing and writing Abstracts/Manuscripts and/or Clinical Trials Protocols. Support the preparation for IRB audit and monitor : + Assist in the preparation of ... Clinical Research Technician/Assistant Apply Now **Job Summary** This position...+ Act as liaison between study team and sponsors, IRB , federal, state, and University officials and other regulatory… more
- University of Michigan (Ann Arbor, MI)
- …of the following: + Minimum 1 years of directly related experience in clinical research and clinical trials is necessary. Please review SoCRA's Definition of a ... Clinical Research Technician Apply Now **How to Apply** A...etc. and assisting with skin biopsies. + Track and monitor participants? condition and test results during the course… more
- University of Michigan (Ann Arbor, MI)
- …of the following: + Minimum 1 years of directly related experience in clinical research and clinical trials is necessary. Please review SoCRA's Definition of a ... Clinical Research Technician Apply Now **How to Apply** A...with preparation, and attend study initiation meetings, audits, and monitor visits. + May work with CTSUs to reconcile… more
- University of Michigan (Ann Arbor, MI)
- …is necessary. + Minimum 1 year of directly related experience in clinical research and clinical trials is necessary. (Please review SoCRAs Definition of ... Clinical Research Technician/ Assistant Apply Now **How to Apply**...data entry system. Coordinate the collection of specimens and monitor study subjects. Ensure integrity of specimens (collection, processing,… more
- Wayne State University (Detroit, MI)
- …collection of essential regulatory documents and the execution of study protocol. Prepare IRB ( Institutional Research Board ) initial applications, ... Clinical Research Coordinator - Department of Psychiatry Wayne State...accurately, in a timely manner per sponsor requirements. Ensure compliance with protocol guidelines and regulatory agency requirements. Collect,… more
- Bausch + Lomb (Lansing, MI)
- …(GCP), clinical trials management (including site monitoring), scientific methods, research design, regulatory compliance , and clinical data management. ... established over our 170-year history. We have a significant global research , development, manufacturing and commercial footprint of approximately 13,000 employees… more