A large medical device company in Irvine, CA is looking for a HYBRID Clinical Research Specialist. This candidate will play a crucial role in supporting a 10 year post market clinical trial for breast implants. Their key responsibilities will include monitoring clinical studies, data verification, regulatory compliance, study documentation, site visits and coordination, and developing written travel reports.
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3+ years of experience as a clinical research specialist/associate or field monitor coming from a background of a large research institution, a sponsor company(medical device / biotechnology / pharmaceutical company) , or a hospital
3+ years of experience working on a clinical trial
Bachelor's Degree
Residing in the mid west / south region of the US
Travel 50%-65%
Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.