Clin Res Assoc I

Job Overview:

Do you have 6-12 months monitoring expereince?  Would you like to work in a dedicated role fully outsourcded in an exclusive role for one single sponsor?  Look no further!

♦ Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, with or without guidance  liaise with vendors 

♦ Responsible for aspects of registry management as prescribed in the project plans

♦ General On-Site Monitoring ResponsibilitiesEducation/Qualifications:

Minimum Required: ♦  University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure) 

Experience:

o A minimum of 2 years of experience in a related role (e.g. site management, in-house CRA, study coordinator, research nurse, etc.)

♦ Basic understanding of ICH Guidelines and GCP including a basic understanding of regulatory requirements ♦ Basic understanding of the clinical trial process ♦ Valid Driver’s License

Preferred: ♦ Working knowledge of Covance SOPs for site monitoring