Cedars-Sinai Clinical Research Coordinator I - Nissen Lab in Los Angeles, California
With surgical and medical expertise in lung, heart, liver, kidney, and pancreas transplantation, the Cedars-Sinai Comprehensive Transplant Center is one of the most successful facilities of its kind. As a Clinical Research Coordinator I, you will 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.
You will be responsible for the accurate and timely processing of source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. Responsibilities also include the compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. You will be expected to present this information at regular research staff meetings. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB).
- BA/BS Degree
- ACRP/SoCRA (or equivalent) preferred
- 2 years of directly related experience
Able to perform moderate lifting.
Able to sit, stand and walk for prolonged periods of time.
Able to read papers and online documents.
Cedars-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.