Clinical Affairs Manager-clinical/regulatory

PLEASE NOTE:  To properly respond, you should format your resume in MS Word or Corel WordPerfect and send it to lar3988@jobquestsite.com .  Visit our website at http://www.jobquestsite.com for other career opportunities. If your qualifications are not a perfect match- send your resume anyway. Opportunities for all levels of quality and regulatory as well as engineering and operations professionals. IMPORTANT! No resume will be sent to Client without your consent. To be considered for this job you must have: Strong Clinical background Must have a comprehensive knowledge of FDA regulations and ISO Experience with IDEs, PMAs, and other FDA submissions At least 2 years experience working with medical related products in clinical/regulatory Engineering, nursing (RN) or biologic life sciences a must- Master’s degree preferred. Ability to manage Clinical Studies DESCRIPTION: Manage and monitor the Clinical Affairs of orthopaedic product manufacturer with 30 years of success in the industry. This could be just the change you need to move your career to next level! Travel required. KEYWORDS: regulatory affairs, compliance, surgical, FDA, orthopaedic, clinical trials, IDE, PMA, 510K, biologics, medical device, clinical Compensation:   High: $95,000.00 plus 10+% Bonus and great benefit package Low: $90,000.00   MRINetwork is the largest and most successful search organization in the world. Each MRINetwork office is a single point of contact to over 1,100 offices in more than 37 countries, our candidates have access to the right jobs virtually anywhere in the world. LOCATION: South Bend, IN JOB CATEGORY: Legal TYPE: Full Time, Employee JOB REFCODE: LAR3988 COMPANY: Management Recruiters of Myrtle Beach, Inc. CONTACT NAME: Lori Rowe, Account Executive EMAIL: Apply by Email