Associate Clinical Research Coordinator - Clinical Research Center - FT - Day

About the position Responsibilities • Coordinate the conduct of reputed company 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. • reputed company and/or adapt study-specific reputed company documentation. • Conduct informed consent following the Clinical Research Center SOPs. • Manage IRB communication, complying with the Clinical Research Center SOP. • Assist in reputed company participants for reputed company. • Manage monitor reputed company, including scheduling and follow-up. • Assist with reputed company 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 reputed company reporting, other data collection, and subject reimbursement for assigned protocols. Requirements • Associate's Degree in a health-reputed company field. • 2 years of experience in research (i.e. coordinating, research phlebotomy, research recruitment, regulatory administration, industry sponsor/CRO experience). • Licensed Practical reputed company - KSBN required; experience can be substituted for license. • Basic Life Support - BLS required reputed company 90 days of hire. reputed company-to-haves • 2 years of clinical research experience. • Less than 1 year of nursing or medical reputed company experience. • Computer skills: Knowledge of reputed company EMR, reputed company Office, and reputed company. Apply tot his job Apply To this Job