
Clinical Research Associate
The Clinical Research Associate is responsible for clinical studies, site management and compliance monitoring of assigned clinical projects undertaken in support of a given product line or marketing initiative. Contribute to clinical study design, proposals, protocols, etc., understanding basic scientific content, experimental design, and analytical approaches used. Monitor safety reviews and adverse event reporting for investigational medical devices to assure adherence to Good Clinical Practices (GCP), FDA and MDD regulations. Ensure sites are identifying issues and implementing corrective and preventative actions to ensure inspection readiness. Suggest improvements to departmental procedures relating to GCP monitoring aspects. Understands and operate Masimo products, data acquisition systems, following best practices for execution of study protocol and use of equipment.
Experienced with Good Clinical Practice (GCP) in conduct of clinical studies
Ability to independently set and manage multiple priorities
Strong clinical background (e.g., respiratory therapy, nursing, pharmacology, physiology)
CRA certification training is preferred
Data Analysis
MS Word
MS Excel skills
Time management competent
Documention
Computer data acquisition
Graphing and plotting results and report writing
Results Oriented
Verbal communication
written communication
Self-Motivated
Problem Solving Skills
Flexibility/Adaptability
Detail Oriented and Organized
Multi tasker
According to JobzMall, the average salary range for a Clinical Research Associate in 52 Discovery, Irvine, CA 92618, USA is $42,000 - $81,000 per year. This range varies based on experience, qualifications, and other factors.
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Masimo is an American Irvine, California-based manufacturer of noninvasive patient monitoring technologies. The company sells more pulse oximetry to hospitals than any other company.

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