CRA-Cutting Edge Device Company with Incredible growth potential!!

Nashville, TN

 

We are consulting on behalf of a growing, Nashville TN medical device organization providing a broad range of products that focus on the repair of orthopedic injuries.

 

Opportunity Statement: 

 

The position, created through organic business growth, will work creatively with research sites to facilitate and supervise the conduct of clinical trials, build relationships, and effectively communicate ideas and results throughout a broad spectrum of organizational levels. 

 

Company Benefits:Extremely competitive salary packageExcellent 401K matchFlexible spendingMonthly financial contribution to employee benefit costStock optionsWireless lap top and Blackberry providedIncredible growth potential and amazing benefits!

Qualifications and Characteristics:Minimum 2+ years of clinical monitoring experienceBachelor's Degree preferred, a degree in Life Sciences or Nursing is a plus!Strong computer skills (MS Office, etc)Excellent communication, presentation, and organizational skillsDemonstrated knowledge of the drug development process, SOP, GCP and other applicable regulationsAbility to travel up to 50% of the time (average of 30-50%)

Responsibilities:Participate in the identification of potential investigators and clinical sites, conduction pre-study site visits, collecting and reviewing data, and preparing evaluative reportsConduct clinical site initiation visits, advising and training site personnel on sponsor and regulatory requirements for study conduct and preparing reportsConduct site monitoring visits to identify significant issues and to ensure that all clinical aspects of the studies are being carried out in accordance with GCP/ICH guidelinesReview on-site files and records, case report forms, and source documents for completeness, accuracy, consistency, and compliance; identify deficiencies and discrepancies, provide remedial training and/or initiate corrective action as requiredProvide site support for remote data capture, monitor data capture remotely, review for completeness and consistency, generate and resolve queries between monitoring visitsAssist in the termination of clinical studies through the oversight of clinical sites through data lock, resolving final queries and completing closeout visits

 

We will only be able to respond to those inquiries who meet the stated requirements.  Please include the position ID (CC-860) in the subject line of your correspondence.  Please forward your credentials in confidence to: recruiter7@ccesearch.com (Word format please).

 

To review additional opportunities, please visit our website at: www.ccesearch.com.