Jobgraze
Coordinates research projects, with applicable research management systems, processes, and monitors progress and completion of clinical studies/trials. May support the design and procurement of funding for new study protocols.
Roles Responsibility
Collaborates with principal investigator, sponsor, and research staff to plan, conduct, and evaluate project protocols. Monitors and reports on progress of projects, as necessary., Conducts informed consent, provides clinical education, performs clinical procedures and other clinical assessments on study participants per the protocol and within scope of practice. Assists with the pre-screening, selection, education, testing and monitoring of research participants., Assesses eligibility of potential participants. Conducts informed consent, utilizes clinical judgment, provides clinical education, performs clinical procedures and physical and other clinical assessments on potential and active study participants per the protocol and within scope of practice., Coordinates with investigator to manage adverse events, compliance, and other participant-related issues. Facilitates the education of necessary parties. Ensures the completion and maintenance of consent forms, case report forms, SAE's and source documents., Within scope of job, requires critical thinking skills, decisive judgement and the ability to work with minimal supervision. Must be able to work in a fast-paced environment and take appropriate action. Desired Qualification
Bachelor of Science in Nursing Type
Full Time
Location
United States, Loveland, CO, 80538 
