



The Clinical Research Associate will independently perform clinical monitoring activities to assure site compliance with study protocols and GCP. Responsibilities include but are not limited to performing all types of monitoring visits, maintaining contact with study sites, report preparation, and communications documentation. As needed, the CRA will assist the Project Managers in the implementation of clinical projects by gathering information concerning therapeutic areas; reviewing protocol synopses and protocols; assisting in the generation of study specific case report forms, source documents and other study tools; identifying investigators and assessing their suitability; assisting in the management of clinical trial medications and supplies; interacting with service providers; and assisting investigative sites with regulatory documentation.
Competitive compensation package commensurate with experience
Participation in Employee Stock Ownership Plan
Please submit your resume to: HR@Jennerex.com
Your resume is very important to us. In order to process your resume in the most efficient manner possible, Jennerex strongly encourages you to apply online. It is not necessary to send a back-up hard copy resume. Thank you for your cooperation with our process and, most importantly, your interest in Jennerex.