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regulatory affairs in Dallas

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  1. Senior Clinical Research Associate

    We are looking for CRAs with at least 6 years monitoring experience and 3-4 years in Oncology .  .   Responsibilities: MONITORING – Preparation, conduct, and reporting of selection, initiation/startup, routine/interim and closeout monitoring visits, Site management, Assistance at internal and third-party audits).  Assures timely reporting of Adverse Events (AE)/Serious Adverse Events (SAE) and protocol deviations.  Maintains regular review of site regulatory binder and ensures proper storage, ...

  2. Director of Medical Staff Services

    Qualifications/Duties   Seeking an experienced leader of Medical Staff Services to join our leadership team as the Director of Medical Staff.  In addition, they will be responsible for overseeing the administrative support of the medical staff, ensuring regulatory compliance, management of the Medical Staff Office, oversight of the credentialing and record keeping for Medical Staff, and the coordination of  hospitals in issues related to Medical Staff. REQUIREMENTS EDUCATION ? Bachelor?s degree in ...