Clinical Trials Associate II

1. Responsible for assisting and providing support to the members of the clinical operations
2. project team (i.e. Clinical Project Managers, Associate Directors, or Directors), in order
3. to facilitate the management of pre- and post-approval clinical trial processes including
4. quality review and document prep.
5. The CTA performs work within established protocols under general supervision

1. Main priority is candidate is competent and able to do this role, and start ASAP.
2. Candidate needs to be able to jump in and do work well.
3. Candidate will be working on documentation review in QC.
4. Candidate must understand clinical trial process and documentation.
5. Must have SOME experience in clinical trial process and documentation.
6. Willing to see new graduates as long as they have some experience.

All your information will be kept confidential according to EEO guidelines.

IF THIS IS THE JOB OPPORTUNITY FOR YOU GIVE ME A CALL AT 646-357-1104 ASAP!

I look forward to hearing from you!