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Franklin Biolabs in King of Prussia, PA, seeks a Scientist, Study Management to perform routine procedures in small and large animal species in a CRO setting, adhering to GLP and Title 21 CFR Part 58. On-site, full-time role requiring strong regulatory knowledge and precise data handling.
Responsibilities include veterinary treatments, rodent colony tasks, data capture in electronic systems, and collaboration across disciplines to ensure study integrity and compliance.
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Full Time Direct King of Prussia, PA, US
30+ days ago Requisition ID: 1071
Fra nklin Biolabs emerges from the esteemed legacy of Dr. Jim Wilson's laboratory, a beacon of innovation in vector technology for over three decades. Building on this rich heritage, Franklin Biolabs is poised to redefine the landscape of the global genetic medicines industry. As a Contract Research Organization (CRO), Franklin Biolabs offers a comprehensive suite of services spanning from discovery through clinical manufacturing. Our goal is to empower our partners by providing unparalleled solutions that drive the advancement of genetic medicines. Leveraging decades of expertise and a commitment to excellence, we bridge the gap between groundbreaking research and ensuring that transformative therapies reach those who need them most.This position involves performing routine procedures in large and/or small animal species in a research Contract Research Organization (CRO) setting. The ideal candidate will bring a strong background in lab animal science, regulatory compliance, communication skills, and attention to detail.
As a Scientist, Study Management, you will independently perform routine procedures in small and/or large animal species while maintaining strict adherence to USDA, FDA, DEA, and institutional (IACUC) guidelines and protocols. Routine procedures include, but are not limited to basic sedation and recovery, blood collection, standard IV dosing, body weights, vitals, blood processing and sample shipment: veterinary treatments. The Scientist, Study Management can also perform rodent colony management tasks such as genotyping, tagging, and weaning.
You will also be tasked with administrative tasks including but not limited to expiration checks, scanning data, filing records, and prepping blood tubes and eppendorfs for sample collection.
All procedures will be documented appropriately in accordance with Title 21 of the Code of Federal Regulations Part 58, which governs the conduct of nonclinical laboratory studies. You will be trained to capture data electronically in a 21 CFR, Part 58 compliant electronic data management system for GLP and MED studies.