Regulatory Specialist

This position is multi-faceted in that the individual will be responsible for the regulatory activities and other administrative duties as assigned. The regulatory responsibilities entail the start-up, maintenance and close out phases of our clinical trials including, but not limited to, the preparation of documentation for regulatory submission to Sponsor/CRO/IRB and ensuring that all aspects of the submission are accurate and complete.

The individual will be dealing with clinical and administrative professionals within CMR and at the Sponsor/CRO/IRB.

This individual should possess strong interpersonal skills and quick communication, as well as be detailed oriented, analytical, and have strong computer skills including Microsoft Office Suite.

A Bachelor's Degree in Business Administration, Communication, or related field is preferred. In lieu of a degree, at least 2 years of regulatory/clinical research experience is required. 

If you are interested in a fast-paced environment at a growing company, then this may be the place for you. We achieve our results by utilizing physicians and individuals who are committed to professional, quality research and by having a process that delivers quality results for sponsors and patients.