Clinical Research Associate Consultant
Advanced Clinical - Bothell, WA

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Job Number: 411668

Clinical Research Associate Consultant

Primary duties/responsibilities:
  • Assist in the oversight of the clinical study conduct, including protocol and CRF development, investigator brochures, ICFs, reports and publications, according to all applicable regulations and company Standard Operating Procedures.
  • Assist in the management of vendors used by the company for all study related tasks.
  • Monitor or co-monitor on an as-needed basis.
  • Perform periodic reviews of CTMF for completeness.
  • Actively participate in study meetings.
  • Provide input on study resource requirements, study budget and timelines. Monitor data flow from sites and CROs.
Experience:
  • 2-4 years of study site monitoring
  • Bachelor's degree in a health profession, science or engineering field or equivalent work experience. Master's degree desirable.
  • Demonstrated proficiency in knowledge of GCPs and knowledge of other pertinent regulatory requirements.
  • Excellent verbal and written communication skills plus computer proficiency (Word, Excel, Outlook) and data management experience.
  • 20%-40% travel required.

Interested candidates please send resume in Word format to dducham@advancedclinical.com Please reference job code 411668 when responding to this ad.

Advanced Clinical - 9 months ago - save job - block
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