
Carrie Angeles
Husbandry Supervisor

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About me
Regulatory Affairs Associate at Fred Hutch
Education

Scotia-Glenville High School
1993 - 1997
SUNY Geneseo
1997 - 2001BS. Biology, Anthropology
Experience

Washington NPRC
Apr 2002 - Jul 2006Husbandry 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 2014Preclinical 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 2018Senior 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 - nowSupport 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 - nowProtocol/Operations Coordinator (Regulatory Coordinator)
Apr 2018 - Jan 2021
Licenses & Certifications

CMAR, RLATG
AALAS.webp)
Certified Clinical Research Professional (CCRP)
Society of Clinical Research Associates (SOCRA)Jul 2021
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