RCRI - Medical Device CRO    
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Principal Advisor

RCRI, a provider of integrated services to the medical device and biosciences industries, is seeking a Principal Advisor.

Responsibilities include initiation, implementation and management of regulatory strategies, submissions and quality compliance activities that meet global requirements.  Duties include designing, managing and/or writing regulatory submissions, advising clients on quality system functions and structure, and coordinating with clinical affairs and biostatistics for support in comprehensive projects, mentoring other RCRI staff, actively pursuing business development and new client opportunities, and marketing RCRI services.  


Qualified applicants will have a degree in a scientific or technical field,  a minimum of twelve years experience in regulatory affairs and quality systems including project management for Class II or Class III devices, excellent analytical and qualitative skills, and a strong understanding of project management. 


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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