Quality Assurance Auditor II/Sr. Quality Assurance Auditor, CQA

We work together to find a better way and break new ground to make progress possible. Focused on common goals, we raise the standard and make a difference. We strive for excellence in everything we do. At ICON, career possibilities can become realities for those who look for challenges and embrace learning and growth opportunities. ICON Clinical Research is dedicated to providing the pharmaceutical and biotechnology industries with exceptional clinical research and biometrics services. Join us in one of our current openings and enjoy highly competitive benefits and exceptional advantages. Quality Assurance Auditor II/Sr. Quality Assurance Auditor, Clinical Quality Assurance (CQA) North Wales, PA Exempt The successful candidate will be responsible for providing assurances of compliance with GCP and other relevant regulatory requirements within ICON as well as investigator site compliance. The QA Auditor II/Sr. QA Auditor will plan, conduct and report internal and external audits independently, or with minimal supervision. In addition, the QA Auditor II/Sr. QA Auditor, CQA will host external audits of ICON including sponsor audits and regulatory audits. Auditors must be detail oriented, able to maintain a ‘big picture’/overview on the project/business, exhibit a high degree of flexibility and initiative, demonstrate the ability to follow-up on multiple tasks and projects, and possess the ability to handle confidential information diplomatically. Auditors will assist with the training of less experienced auditors and will provide direction and coordination for project activities related to assigned areas. The position will also include providing advice on regulatory compliance. Position will involve approximately 35% travel on average. The qualified candidate will have a Bachelor's degree in the Life Sciences, or related discipline, or a mix of relevant equivalent college and experience to such a four year degree. Must have experience and knowledge of FDA/GCP regulations and ICH/GCP guidelines and relevant clinical trial regulations and laws. Must possess excellent communication and organization skills. Must possess the ability to manage multiple and varied tasks and to prioritize workload. Must possess excellent time management skills and the ability to follow-up on multiple tasks and projects. A Minimum of two years GCP auditing experience is required. **The level of position will be dependant on the experience level of the candidate** Come to ICON and be an important part of a well respected and growing company that believes the details of your career are every bit as critical as the work you do. You'll enjoy highly competitive benefits in addition to flexible scheduling, relocation assistance, tuition reimbursement, credit union, health club privileges, and many other exceptional advantages. TO APPLY and for more information on our opportunities and locations, please visit us at http://www.iconclinical.com/index.asp?getpage=true&sid=10 . No agencies, please. ICON. A Symbol of Excellence. ICON Clinical Research is an Equal Opportunity Employer committed to strength in diversity. To Apply for this position, please CLICK HERE