158 information-security-"https:"-"https:"-"https:"-"https:"-"https:" positions at Cedars Sinai Medical Center
Sort by
Refine Your Search
-
. Demonstrated aptitude to perform experimental protocols and procedures, including detailed data collection, and analysis and operation and maintenance of specialized equipment. Knowledge of safety standards and
-
and detailed records of experiments and results, assists in the operation of specialized equipment and machinery, and observes safety standards and procedures. This position does not have supervisory
-
implement the study. This role evaluates and abstracts research data and ensures compliance with protocol and research objectives. Position is responsible for completing case report forms, entering clinical
-
. This shared culture of happiness, passion, and dedication pulses through Cedars-Sinai. We invite you to consider this phenomenal opportunity! Dr. Pramod Butte, Ph.D. is looking for a Clinical Research Associate
-
Description The Applied Genomics, Computation & Translational Core is looking for a Biomedical Technician to join the team! The Cedars-Sinai Applied Genomics, Computation & Translational (AGCT) Core is an
-
Save Job Employees: Apply Here Job Description Principal Investigator, Shouri Lahiri, MD is seeking for a motivated Research Associate III to join his team! The Research Associate III works closely with
-
safety standards and procedures, assist in preparation of data for publication and/or presentation at scholarly meetings, and assist in general laboratory maintenance. This position does not have
-
in tasks supporting the coordination/implementation of noncomplex research studies. Supports objectives of research studies through noncomplex tasks such as data collection, prescreening of potential
-
Description This is a full-time, onsite position, with a Monday–Friday work schedule. Ideal candidates will have some experience working with laboratory mice, including (but not limited to) animal care and
-
of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate and timely source documents, data