Coloradoacc
Staff Research Associate/ Study Coordinator 3 - Cardiology
Coloradoacc, Los Angeles, California, United States, 90079
Description
Play a key role with a world-renowned leader in medical research. Help advance medical knowledge and leading-edge patient care. Take your career to a higher level. You can do all this and more at UCLA Health.As a Study Coordinator in clinical research, you will be responsible for human subject recruitment, screening, enrollment, and retention. The role will involve applying your skills in organizing, analyzing data, generating summary figures, and preparing presentations and manuscripts. You will need to be proficient in the use of image post-processing (e.g., MRI, cardiac ultrasound, echo, etc.) and measurements. You will also assist with image measurements, database management, and ordering laboratory animals and supplies.Salary: $5,536.68- $8,903.58 annuallyQualifications
We’re seeking a self-motivated, independent professional with:
Five or more years of experience as a study coordinator for clinical researchData management experience with clinical research protocolsKnowledge of health services or clinical research methodology and principlesIRB experience and coordination of clinical studies preferredBackground in ARC and pre-clinical large animal studies desiredExperience following strict research imaging protocols and data entryExceptional writing skills, including the co-authorship or authorship of research or technical reportsComputer proficiency with Microsoft Office, STATA, SAS, Illustrator, Mimics, etc.Familiarity with basic statistical tests and proceduresKnowledge of the rules and regulations for Human Subject Protection and informed consent
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Play a key role with a world-renowned leader in medical research. Help advance medical knowledge and leading-edge patient care. Take your career to a higher level. You can do all this and more at UCLA Health.As a Study Coordinator in clinical research, you will be responsible for human subject recruitment, screening, enrollment, and retention. The role will involve applying your skills in organizing, analyzing data, generating summary figures, and preparing presentations and manuscripts. You will need to be proficient in the use of image post-processing (e.g., MRI, cardiac ultrasound, echo, etc.) and measurements. You will also assist with image measurements, database management, and ordering laboratory animals and supplies.Salary: $5,536.68- $8,903.58 annuallyQualifications
We’re seeking a self-motivated, independent professional with:
Five or more years of experience as a study coordinator for clinical researchData management experience with clinical research protocolsKnowledge of health services or clinical research methodology and principlesIRB experience and coordination of clinical studies preferredBackground in ARC and pre-clinical large animal studies desiredExperience following strict research imaging protocols and data entryExceptional writing skills, including the co-authorship or authorship of research or technical reportsComputer proficiency with Microsoft Office, STATA, SAS, Illustrator, Mimics, etc.Familiarity with basic statistical tests and proceduresKnowledge of the rules and regulations for Human Subject Protection and informed consent
#J-18808-Ljbffr