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.ppd_header {width:748px;margin-left:auto;margin-right:auto;}.ppd_body {width:748px;margin-left:auto;margin-right:auto;}.ppd_left {background-color:#E1E2E4;width:135px;}.ppd_text {background-color:#FFFFFF;padding:10px;width:586px;}.ppd_right {background-color:#E1E2E4;width:27px;}At PPD, you'll have the freedom to try new ideas and the ability to do something truly great. In our environment, innovation is encouraged. That's why the world's leading pharmaceutical and biotechnology companies come to us for discovery and development services. And why PPD is the best choice for you and for your career. Sr. CRA - CENTRAL U.S.DescriptionThe Sr. Clinical Research Associate (CRA) performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and PPD Standard Operating Procedures. Conducts site visits to assess protocol and regulatory compliance and manages required documentation Responsible for ensuring that data will pass international quality assurance audits. Represents PPD in the global medical research community and develops and maintains collaborative relationships with investigational sites and client company personnel. May assist project manager or clinical team manager on assigned projects. Required to travel 60-80% on average.Qualifications Education and Experience: Bachelor's degree in a science related field or a Registered Nursing certification or equivalent certification/licensure from an appropriately accredited institution Previous experience as a clinical research monitor (comparable to 2+ years) that provides the required knowledge, skills and abilities Valid Driver's License where applicable In some cases an equivalent combination of education, professional training, and experience that provides the required knowledge, skills and abilities may be considered Knowledge, Skills and Abilities: Effective clinical monitoring skills�10;Demonstrated understanding of medical/therapeutic area knowledge and medical terminology Excellent understanding and demonstrated application of Good Clinical Practices and applicable Standard Operating Procedures Effective oral and written communication skills, with the ability to communicate effectively with medical personnel Strong customer focus Effective interpersonal skills Strong attention to detail Effective organizational and time management skills Proven flexibility and adaptability Ability to work in a team or independently as required Good computer skills: good knowledge of Microsoft Office and the ability to learn appropriate software Good English language and grammar skills Good presentation skills PPD is an Equal Opportunity EmployerAdditional InformationPosition Type: Full Time, EmployeeRef Code: 00628