Clinical Research Associate Jobs

Role: Clinical Coordinator

Location:Maple Grove, MN (will be on-site for the first month for training and then based on competency of performance, those doing well will be allowed to work from home for the rest of the contract and those not performing well will be asked to continue to go into the office)

Duration:04-05 months Contract, may extend further depends on the business need of project and performance.

Position Description

Look for candidate who has some documentation and some clinical research experience and computer savvy

will be reviewing regulatory documents, uploading, filing them and moving to their program.

System used is called CDO Gateway for the regulatory docs - medical documents experience is NOT required

Must have Computer experience and be well versed in MS office suite, including Outlook, Excel, Work, pdf - Adobe,

Must be self-motivated, analytical, organized, and exercise accuracy

Preferred years of experience is 2 plus in similar role where they have conducted document reviews and have clinical knowledge

Will accept Associate, Bachelors, Masters and fresh college graduates with a discipline in some type of clinical field

Nurses are okay if they are trying to transition away from nursing

Will consider someone with No College Degree as long as they have the necessary experience

A degree is preferred given the high level of FDA regulatory documents they will be working with