The position is responsible for performing on-site monitoring activities to ensure that the clinical study is conducted in accordance with approved protocols, applicable regulations, work instructions and guidelines. This position will assist with the design, development and monitoring of clinical evaluation projects and associated monitoring plans.

Qualifications:
Requires a four-year degree in nursing, cardiovascular or a technical discipline (or equivalent) and a minimum of 3 - 5 years of work experience in a hospital/clinic cardiovascular setting (operating room environment) with 2 of the 3 - 5 years work experience including the monitoring Class III medical device studies. Requires advanced written and oral communication skills, the ability to manage multiple tasks and a proficient knowledge of medical terminology.




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Clinical Studies Monitor - Michigan

For more information, or to submit your resume, contact Suzanne Steele.