Carrie Angeles

Carrie Angeles

Husbandry Supervisor

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location of Carrie AngelesEverett, Washington, United States

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  • Timeline

  • About me

    Regulatory Affairs Associate at Fred Hutch

  • Education

    • Scotia-Glenville High School

      1993 - 1997
    • SUNY Geneseo

      1997 - 2001
      BS. Biology, Anthropology
  • Experience

    • Washington NPRC

      Apr 2002 - Jul 2006
      Husbandry Supervisor

      -Supervision of an animal husbandry staff of twenty-five-Assign work schedules; train new employees-Work with research and veterinary staff on specific animal issues-Maintain animal records and inventory of supplies-Receive and distribute animals from procurement sources

    • Amgen

      Jul 2006 - Dec 2014
      Preclinical Manager

      -Supervision of husbandry staff and departmental operations-Coordinate technical services for investigative staff -Ensure compliance with regulatory guidelines and requirements, departmental guidance documents, company safety procedures, and animal use protocols-Conduct performance reviews and maintain training records; handle disciplinary procedures as necessary-Recruit and train new employees-Procure and maintain operational supplies

    • Allen Institute

      Mar 2015 - Apr 2018
      Senior Project Coordinator

      -Conduct performance reviews and performance development; handle disciplinary procedures as necessary; Hire staff as necessary-Coordinate scheduling of day-to-day tasks, assign work hours and create task rotation schedule-Ensure compliance with animal use protocols and Institute standard operating procedures; write and review SOPs and departmental work instructions; participate in semi-annual IACUC inspections and program review-Prepare the departmental yearly budget plan; provide input to Institute yearly project plans-Improve Department processes to promote animal welfare and capture innovation and efficiency; standardize pre-and post-operative care for all surgical animals Show less

    • Fred Hutch

      Apr 2018 - now

      Support of the Institution-Sponsored IND Program:-create, review and submit regulatory packets to the FDA-facilitate SAE processing-monitor visit preparation and follow up-assist with development and implementation of SOPs Clinical Trial Support:-Prepare IRB documents for local and central IRBs for national cooperative group clinical trials. -Prepare IRB documents and other study-related tools for the start-up and management of clinical trials.-Write and review SOPs

      • Regulatory Affairs Associate

        Nov 2020 - now
      • Protocol/Operations Coordinator (Regulatory Coordinator)

        Apr 2018 - Jan 2021
  • Licenses & Certifications

    • CMAR, RLATG

      AALAS
    • Certified Clinical Research Professional (CCRP)

      Society of Clinical Research Associates (SOCRA)
      Jul 2021