As a Clinical Research Coordinator Il, you will work independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.
Will be responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries.
Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings.
You will ensure compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB).Educational Requirements:+ BA/BS Degree is requiredLicense/Certification/Registration Requirements:+ Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associate (SOCRA) certification strongly preferred.Experience:+ Four (4) years minimum of directly related experience.+ Must demonstrate excellent communication, computer(excel, powerpoint, word), written,verbal, and organization skillsCedars-Sinai is an EEO employer.
Cedars-Sinai does not unlawfully discriminate on the basis of the race, religion, color, national origin, citizenship, ancestry, physical or mental disability, legally protected medical condition (cancer-related or genetic characteristics or any genetic information), marital status, sex, gender, sexual orientation, gender identity, gender expression, pregnancy, age (40 or older), military and/or veteran status or any other basis protected by federal or state law.