Full Job Description
The Research Associate serves as a member of the clinical research team and provides research expertise in the day-to-day management of the clinical research program; including patient eligibility assessment, safety assessment, regulatory compliance, Institutional Review Board functions, and administrative issues involved in opening and maintaining industry, cooperative group and investigators initiated trials.
Educational Skills Required (Degree(s), Certification(s), License, etc.)
Bachelors degree required; Certification through Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals(ACRP), preferred.
Work Experience Required
2+ years experience in clinical research, preferably in an oncology setting. Study Coordinator certification (CCRC) is preferred with 2 - 4 years of experience in the oversight of oncology clinical trials. Computer knowledge, using Word, Excel, Power Point, Internet.
Location: Trinitas Regional Medical Center · 72600 - CANCER CTR - GENR
Schedule: Part Time - Less than 30 Hours/week, Days, typically 3 days a week depending on work needs