Clinical Research Regional Monitor - East Coast

JOB SUMMARY:

Implement and carry out monitoring functions for clinical research studies.  Schedule and monitor monitoring activities at assigned centers assessing site compliance to the clinical investigation plan, regulations and Good Clinical Practices.  This position is related to increased monitoring for post-market and pediatric studies.  Travel is about 50-75% in eastern part of US.  Can be based in Washington DC or Raleigh NC.

 

BACKGROUND REQUIRED:BA/BS in Medical Science, Nursing or related field2+ years experience in clinical research, preferably medical deviceKnowledge of clinical research study processes and study design and ability to incorporate and adhere to GCPs, regulatory standardsComputer proficiency - MS Office, database systems, internetAbility to produce professional correspondence, presentations, reports and training materialsAbility to recognize reportable adverse events when reviewing patient charges, ensuring that proper IRB/FDA requirements have been followed.Ability to interact with internal and external teams and to work independently (desire experience working from home base)Attention to detail, ability to organize, prioritize and manage teamsCurrent, valid driver’s license

 

Email WORD resume to:  Phyllis.wright@entegee.com .  Refer to Job#456283pw.