As Clinical Research Coordinator, you will instruct and coordinate all aspects of research-related activities, including recruitment and evaluation of study patients. Your responsibilities will include coordinating the IRB and CRP processes, facilitating data collection and analysis, writing research abstracts, and providing related support. You will act as the primary administrative point of contact for the principal investigators and any research assistants participating in the registry.
The successful candidate must have at least 2 years experience in Clinical Research. Strong organizational and problem solving skills as well as excellent written and communication skills are essential. Proficiency in Microsoft Office Suite and Database experience is required. Bachelor degree required. Expectation of CRC Certification to be obtained within 2 years.