Description
The Clinical Research Associate helps manage multi-site medical device clinical trials in compliance with GCP, ICH, and company SOP's.
Main responsibilities include:
Managing multi-site recruitment activities; Generating training material for device studies; Creating product education materials for patients, physicians and Clinical Research Organizations (CROs); Managing CRF data and product data analysis; Maintaining Trial Master Files; Implementing patient recruitment projections; Contributes to FDA annual reports; Assists with management of CRO's, site monitoring, and other third party vendors; Manages and coordinates study supplies and device accountability
Education / Experience:
Bachelors Degree, Life Sciences preferred; 3+ years experience as a CRA within the Medical Device or Pharmaceutical industries; Ability to travel up to 20%; Basic knowledge of medical terminology; Ability to effectively work independently; Excellent verbal and written communication skills plus computer proficiency (Word, Excel, Outlook) and data management experience
To find out more about Real, please visit www.realstaffing.com