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| This position will lead a group to provide analytical research in support of projects arising from ... |
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| Process Engineer |
| PROCESS ENGINEER
Linco Research in St. Louis MO, now a part of Millipore, is a leader in ... |
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| OPERATIONAL EXCELLENCE LEADER |
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| Field Service Engineers Boston & St. Louis |
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| Responsible for all aspects of the development, implementation, and maintenance of the radiation ... |
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| HEALTH PHYSICIST |
| RESPONSIBILITIES FOR PHARMACY RADIATION SPECIALIST - HEALTH PHYSICIST AT TYCO HEALTHCARE/MALLINCKROD... |
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| QUALITY TECH III |
| QA Auditor for the QA Operations Group
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-Perform room ... |
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| Designs building facilities, equipment, and machinery. Coordinates with building contractors and ... |
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LOOKING FOR 6 REGULATORY COORDINATORS
| Details |
Country: USA
Location: MO Kansas City
Total applied: 19
Relevant Work Experience: 2+ to 5 Years
Career Level: Experienced (Non-Manager)
Education Level: Bachelor's Degree
Job Type: Temporary / Contract / Project
Job Status: Full Time
Job Shift: First Shift (Day)
Salary: From 20.00 to 30.00 USD per hour
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LOOKING FOR 6 REGULATORY COORDINATORS
Excellent Regulatory Document Coordinator Opportunity in KC, Missouri
Study Start-up Experience HIGHLY Desirable
Qualified Individuals will audit documents against source material, instructions and checklists for accuracy, completeness and consistency. Will contact site personnel for missing, incomplete and inaccurate documents and provide instruction on completion.
MUST HAVE VALIDATION EXPERIENCE IN REGULATORY (not just of CRF's or queries, but with Clinical Documents, such as: informed consent, HIPAA, 1572s, CVs, protocols, amendments.) Review of study documents from a content perspective. Specific experience in investigator contract and budget negotiations, without regulatory document review experience, would be acceptable.
Any study site start up experience would be a big plus.
Requirements: Degree preferred. Must have Regulatory Data Review experience (minimum 6 months).
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Biotechnology and Pharmaceutical 
