Homebased CRA / Sr. CRA
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Company: Quintiles
Contact Name: Mike Lendach
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- Job ID:8915
- Date:06/27/2008
- Location:Reno
- State:Nevada
- Degree:B.S./B.A.
- Current Professional Level:Experienced Staff Level
- Additional Salary/Compensation:
- depends on experience
- Job Types:
-
Clinical Research Associate
Job Description
The Clinical Development Services division of Quintiles has more depth of therapeutic expertise and a broader range of services than any other service provider. We conduct both US and Global trials in all therapeutic areas. In fact, Quintiles conducts more clinical trials than anyone else in the world. Become involved in work that improves the quality of life for people around the globe. Let your career soar! We are seeking an enthusiastic CRA to join the team in our San Diego CA office.
The Clinical Research Associate monitors activities at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs, and study protocols. Review regulatory documents as required and prepare site visit reports. Responsible for multiple projects and must work both independently and in a team environment. May participate in the study development and start-up process including reviewing protocols, designing and/or reviewing CRFs, preparing Informed Consent forms, developing study documents, organizing and presenting at investigator meetings, working with management on monitoring strategy, and/or developing project-specific CRA training. Participate in clinical training programs and maintain awareness of developments in the field of clinical research.
Position will be filled at CRA or Sr CRA level depending on education and experience.
QUALIFICATIONS:
- Customer service orientation - Sound knowledge of medical terminology and clinical monitoring process - Ability to perform regionalized travel an average of 65%, depending on project needs. - Excellent verbal and written communications skills - Excellent interpersonal and organizational skills and attention to detail - Computer literacy, proficiency in MS Office
BS/BA and 1 year clinical monitoring experience, OR Associates degree and 3 years experience in clinical research with a minimum of 1-1/2 years of monitoring, OR a high school diploma and 6 years related experience with a minimum of two years of monitoring.
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