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regulatory affairs in Kansas City

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  1. Bio Clinical Development Senior Scientist

    The Biological Clinical Development Scientist will provide pivotal and non-pivotal clinical trial study design and implementation for cattle, swine and companion animal vaccine projects; including safety, field safety and efficacy.  The incumbent will serve as clinical core team member and the functional clinical leader on project teams from Research to Market Support vaccine projects, with an emphasis on pivotal studies in development to earn new product licenses and label claims. The incumbent ...

  2. Regulatory Affairs

    HRC 05-20RETAINED SEARCH ASSIGNMENTTitle: Regulatory Affairs, Sr. ManagerProvides regulatory strategy, support, and governance for veterinary pharmaceutical products – both pre market (development) and post market … ensuring drug product regulatory compliance at the federal, state and local levels.  MUST possess detailed knowledge of FDA/CVM regulations with regard to drug development, registration, and life cycle management.  Experience in conduct of FDA regulatory registrations and maintenance of ...

  3. 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, ...

  4. Senior Clinical Research Associate

    We are looking for Midwest 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 ...

  5. Plant Quality Manager - located in Centralia, IL

    On January 29, 2014, Pinnacle Foods Inc. (NYSE: PF) (“Pinnacle Foods”) entered into a definitive agreement with Duncan Hines co-packer Gilster Mary Lee (“Gilster”) to acquire the Duncan Hines manufacturing business located in Centralia, Illinois. Duncan Hines manufacturing has been under a long-term co-packing contract with Gilster since 1998, and the Centralia facility has only produced Duncan Hines products since that time. The acquisition will enable Pinnacle to cost-effectively invest in the ...