US - Houston, Texas |
Requirements: a minimum of 10 years experience preferably in a CRO environment, the ideal candidate will be responsible for developing and enhancing worldwide clinical quality assurance policies. Monitoring and tracking ongoing studies' clinical quality assurance compliance with regard to GCPs, SOPs, EU directives, and national and local guideline and laws. The ideal candidate must have extensive knowledge of GCP and be available to travel. This is a full-time position is based in our Houston office. If you have the right qualities and thrive on challenges then please apply to shari.milligan@pharm-olam.com PRINCIPALS ONLY. NO PHONE CALLS PLEASE.
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