Location: Candidates local to Irvine, CA are preferred. Will consider 100% remote for the right individual.
Duration: 1 year+
Start Date: 3/20
Job Description: Our client is seeking a Lead Clinical Research Consultant to support a ischemic stroke related device study. This individual will be responsible for managing sites, assisting with ICF & protocol review, and supporting site start-up. The Lead Clinical Research Consultant will help provide guidance to other team members, and work cross-functionally with Physicians.
Skill and Experience Requirements:
Clinical Operations
IRB Submissions
CRA Management
Site Management & Vendor Management
ICF & Protocol Review
Direct experience working on device studies (preferred), Site Selection.
Having device and/or stroke experience is a plus.
Having site start up experience is a plus.
Education: Minimum of a Bachelor’s Degree preferably in Life Science, Physical Science, Nursing, or Biological Science required.
Lead Clinical Research Consultant (232872) Will consider 100% remote for the right individual
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