Multiple Clinical Research Positions
Los Angeles, CA
Providing healthcare for more than 100 years, Cedars-Sinai has evolved into one of the most highly renowned medical centers in the world. Cedars-Sinai has one of the largest state-of-the-art clinical research trial facilities of any private hospital in the nation. Our facility is a testament to the Medical Center’s commitment to remain on the forefront of applying research discovery to patient care. The greater Los Angeles area in which Cedars-Sinai resides possesses unparalleled cultural and ethnic diversity which offers outstanding opportunities for translational and clinical research and a dynamic environment for medical education.
Our clinical trials may seek to discover new drugs, new ways of giving patients approved drugs, new combinations of approved drugs, novel therapies, new surgical techniques, devices or biological products. Some of our institutes involved in clinical trials are: Cancer, Heart, Neurology and Lung.
We have multiple clinical research openings:
Clinical Research Associates - evaluates and abstracts clinical research data from source documents. Ensures compliance with protocol and overall clinical research objectives. Requires the minimum of a Bachelor’s degree or equivalent combination of education and experience and understanding of general research objectives (refer to requisition #25627).
Clinical Research Coordinators – works independently by providing study coordination that includes screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to patients and participating in the informed consent process. Requires the minimum Bachelor’s degree and at least two (2) years of directly related experience. SOCRA/ACRP or equivalent certification, preferred (refer to requisition #25297, 24774).
Clinical Research Budget Coordinators – develops clinical trial budgets. Evaluates research protocols to assess resource needs, cost allocation, negotiates and details budgets. Requires the minimum of a Bachelor’s degree, and at least two (2) years of directly related experience. SOCRA/ACRP or equivalent certification, preferred.
Regulatory Coordinators – prepares and submits protocols and other documents to regulatory bodies such as PRMC, IRB and IACUC. Completes forms and generates reports to comply with regulatory requirements and institutional policies. Requires the minimum of a Bachelor’s degree with at least one (1) year of directly related experience (refer to requisition #24483, 22251,22950).
Other Clinical Research positions include Research Nurse Coordinator (Req#22263, #25345), Clinical Research Specialist (Req#20897), Clinical Research Data Specialist, Grant and Contracts Officer, IACUC Analyst, Financial and Management Analyst (Req#25422) and IRB Analyst (Req#25077), and others.