Senior Clinical Research Coordinator

Location
Irvine
Posted
Jul 06, 2018
Institution Type
Four-Year Institution


University of California, Irvine

Senior Clinical Research Coordinator


Provides support, coordination and leadership for drug studies that may involve industry-sponsored Phase II, III, and IV clinical trials, government-funded clinical research, and investigator-initiated clinical research. Ensures smooth, accurate progress of clinical studies from the planning and approval stages through study completion and post-study closure. Prepares documentation for submission for review by the Institutional Review Board (IRB), recruits and screens study participants, coordinates their clinical treatment and follow-up care, and helps facilitate their continued participation; abstracts data from medical records and other sources; collects, submits and maintains study data and regulatory documents; develops and ensures compliance with study protocols; acts as liaison between study sponsor, contract research organization (if applicable), site PI, and patients.

The University of California, Irvine is an Equal Opportunity/Affirmative Action Employer advancing inclusive excellence. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected categories covered by the UC nondiscrimination policy.

Salary: Monthly $5,450.00 - $6,850.00
Total Hours: 8-5, M-F
Career Position.
Final candidate subject to background check.
As a federal contractor, UC Irvine is required to use E-Verify to confirm the work status of individuals assigned to perform substantial work under certain federal contracts/subcontracts.
Please attach your resume.

Click here to see the Neurology website.

View Job Description for the position requirements.


To apply, visit https://staffing2.hr.uci.edu/CSS_External/CSSPage_Referred.ASP?Req=2018-0757

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