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Tue, Apr 15 2014
Senior Clinical Research Associate  South San Francisco, CA
Posted on: BioSpace
Description: One of our clients is seeking a highly experienced Senior CRA with in-depth knowledge of Phase I through III Clinical Trials. The applicant will collaborate together with the Clinical Program Manager, be responsible for the planning, implementation, monitoring and site management of clinical studies. The applicant must have in-depth background in conducting pre-study, site-initiation, monitoring, and closeout visits. The applicant may be responsible for training of CRAs/CRO in conduct of such visits. Responsibilities may include managing clinical supplies, working with/managing CROs, recruiting investigators, organizing investigator meetings, setting up internal central systems as needed, assist in writing study protocols, final study reports, SOPs, expedited/annual safety reports, and designing and implementing CRF's. Duties also include liaison activities with manufacturing and multiple project group members. Position qualifications: Requires a BS, RN, or RPh and 5+ years of related clinical background. Requires knowledge of FDA, ICH and GCP guidelines. This is a very hands-on position in a very small start-up clinical group. Expertise to operate independently, excellent interpersonal and communication abilities are critical, as is flexibility and strong attention to detail. Expertise to travel when required To find out more about Real please visit  .... (see more)
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