Clinical (GCP) QA Auditor - Mid to Senior Level - Pharmaceutical / CRO $$

Our client, a growing CRO located near Research Triangle Park, is actively recruiting for a seasoned QA professional for key role on its expanding Quality Assurance team.  The Firm is experiencing tremendous growth and they are eager to bring on a sharp and knowledgeable quality professional to lead their GCP efforts.  This position is a direct hire position that will require minimal travel.

 

The selected candidate will be responsible for responding to and preparing for audits done by the clinical trials Sponsor.This organization is looking for a strong clinical professional with extensive GCP experience to assume this challenge.  In addition to the requisite technical skills/experiences noted below, client seeks a candidate who has the ability to think quickly, pay strong attention to detail, trouble shoot when needed, direct others and work independently. 

 

The ideal candidate will have 7+ years of experience in the pharmaceutical, biotechnology or CRO industry and have 3 to 5 years of experience as a QA Auditor.  The select candidate MUST have extensive knowledge of ICH, GCP and relevant regulations and must be familiar with concepts, practices and procedures, as well as all aspects of clinical trials.  BA / BS is required and RAC &/or CQA certifications is a plus.

 

If you are interested in the opportunity, please submit your Word CV to jessical@frankelstaffing.com