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Franklin Biolabs in King of Prussia, PA, is seeking a Senior Scientist, Study Management to lead and perform complex in vivo procedures across small and large animal species in a CRO setting, ensuring USDA, GLP, DEA and IACUC compliance.
You will serve as SME, supervise staff, train newcomers, develop study execution plans, review protocols, and help create SOPs to align with regulatory requirements; on-site role with potential travel.
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Full Time Direct King of Prussia, PA, US
2 days ago Requisition ID: 1081
Franklin 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.
The Senior Scientist, Study Management position plays a central role in executing and overseeing complex in vivo procedures across small and large animal species in a Contract Research Organization (CRO) setting. The ideal candidate will bring a strong background in vivo techniques, regulatory compliance, and will act as a subject matter expert (SME).
As a Senior Scientist Study Management, you will independently perform routine and specialized procedures in small and large animal species while maintaining strict adherence to USDA, GLP, DEA, and institutional (IACUC) guidelines and protocols. Specialized techniques may include, but are not limited to various behavior testing, complex procedures (such as cerebral spinal fluid collection), and various imaging techniques (such as echocardiograms) while ensuring accurate dosing documentation and real-time monitoring of animal responses.
You will act as the primary technical supervisor for assigned active in vivo research studies in partnership with In Vivo Services leadership. This includes developing execution plans, ensuring study milestones are met, and coordinating with cross-functional teams to maintain study continuity. Provide training and technical guidance to new and junior staff. Act as a SME for complex procedures and ensure best practices are followed.
This position will also involve other administrative duties including reviewing and editing study protocols for proposed research projects, maintaining and updating study-specific documentation, and developing Standard Operating Procedures (SOPs) as necessary to ensure current procedures align with regulatory and operational requirements.
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.
All responsibilities are expected to be performed with minimal instruction, and you are expected to independently perform duties as described.
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