Job Description
About the position Responsibilities • Coordinate the conduct of clinical trials adhering to the protocol and coordinating the research subject through the protocol requirements and schedule. • Coordinate subject identification and eligibility activities, including database lists, incoming calls and inquiries, telephone screening, chart reviewing, discussing the protocol with prospective subjects, presenting/re-presenting candidates to PIs and Sub-I's, and scheduling per protocol requirements. • Develop and/or adapt study-specific source documentation. • Conduct informed consent following the Clinical Research Center SOPs. • Manage IRB communication, complying with the Clinical Research Center SOP. • Assist in recruiting participants for clinical trials. • Manage monitor visits, including scheduling and follow-up. • Assist with quality assurance to ensure credentialing as a study site. • Document and address Adverse Events, IND Safety Letters, and Serious Adverse Events per Clinical Research SOPs and sponsor requirements. • Manage drug accountability, case report form reporting, other data collection, and subject reimbursement for assigned protocols. Requirements • Associate's Degree in a health-related field. • 2 years of experience in research (i.e. coordinating, research phlebotomy, research recruitment, regulatory administration, industry sponsor/CRO experience). • Licensed Practical Nurse - KSBN required; experience can be substituted for license. • Basic Life Support - BLS required within 90 days of hire. Nice-to-haves • 2 years of clinical research experience. • Less than 1 year of nursing or medical professional experience. • Computer skills: Knowledge of EPIC EMR, Microsoft Office, and Outlook. Apply tot his job