Clinical Trials Associate II

Responsible for assisting and providing support to the members of the clinical operations project team to facilitate the management of pre- and post-approval clinical trial processes including quality review and document prep.

Requirements

• Candidate needs to be able to jump in and do work well.
• Candidate will be working on documentation review in QC.
• Candidate must understand clinical trial process and documentation.
• Must have SOME experience in clinical trial process and documentation.