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The Investigator (MD or DO) will be responsible for ensuring that Phase I Investigations are conducted according to signed investigator statement, protocol, Standard Operating Procedures (SOPs), Good Clinical Practices (CGPs) and FDA regulations. The investigator is responsible for ensuring participant safety throughout the study. Also responsible for providing medical consultation to scientific staff and study sponsors relating to design, implementation, conduct and report of research studies.
Successful candidate must have a current/valid state medical license with a board certification in a specialty recognized by the American Board of Medical Specialties. Experience in clinical research is a plus. ACLS or CPR Certification is required. EOE