RCRI - Medical Device CRO    
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Regulatory Affairs Regulatory Affairs
Clinical Trial Design & Management Clinical Trial Design & Management
Database Development & Compliance Database Development & Compliance
Reimbursement Strategy and Implementation Reimbursement Strategy and Implementation
Health Economics Health Economics
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Clinical Monitor II

RCRI, a provider of integrated services to the medical device and biosciences industries, is seeking a Clinical Monitor/II.

Responsibilities include the oversight of all aspects of a clinical study.  Duties include performing site qualifications, site initiation, monitoring, study close-out, preparing study progress reports, file maintenance, data validation, and monitoring or auditing for compliance with clinical protocol.  Qualified applicants will have a BS/BA in a health/sciences related field (or equivalent experience), excellent communication skills, previous monitoring experience, two years to four years of medical device clinical experience preferred as well as the ability to work independently and on a team. This position requires 70-80% travel. RCRI offers a progressive work environment including flexibility and comprehensive medical, dental, retirement and profit-sharing benefits.  Forward resume with salary requirements to: hr@rcri-inc.com  RCRI, Inc. 5353 Wayzata Blvd., Suite 505, Minneapolis, MN  55416.  No phone calls, no agencies please. EOE














 

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