Jennifer Crawford, CCRC, CCRA
Sr. CRA @ CoMind
About
With over 25 years of clinical research experience, I am familiar with numerous aspects of the clinical trial industry. I have experience in site coordination, clinical monitoring and regulatory submissions. I am a highly motivated individual with extensive knowledge of GCP, ICH, ISO and FDA regulations.
United States
Fort Worth
Research
Written Communication, Site Management, Site Documentation, Memos, Informed Consent, IT Escalation, General Correspondence, Quality Control, Trial Master File (TMF), Quality Auditing, Project Documentation, Tracking Systems, Tenacious Work Ethic, Oral Communication, Attention to Detail, Query Writing, Query Resolution, Problem Solving, Phase II, English
Experience
Jennifer Crawford, CCRC, CCRA's Contact Information
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