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. Franklin Biolabs, Inc. is in search of a Scientist II which involves performing and overseeing specialized procedures in either small or large animal species in a research Contract Research Organization (CRO) setting. The ideal candidate will bring a strong background in in vivo techniques, regulatory compliance, and rodent colony management, and will act as a subject matter expert and mentor to junior staff. As a Scientist II you will independently perform routine and specialized procedures in either small or large animal species while maintaining strict adherence to USDA, FDA, DEA, and institutional (IACUC) guidelines and protocols. Specialized techniques may include, but are not limited to: various behavior testing, echocardiograms, electrocardiograms, nerve conduction studies, optical coherence tomography, ultrasonography, fluoroscopy, cerebral spinal fluid collection, venipuncture, capillary blood sampling and blood draws from venous access devices. You will also be responsible for administering vectors and compounds via various routes including oral, intrathecal, intraocular, intramuscular, subcutaneous, and intravenous. Ensure proper dosing documentation and monitoring of animal responses in accordance with study and IACUC protocols. You will act as a Study Lead on assigned projects. This includes coordinating and overseeing scheduled procedures, ensuring study milestones are met, and maintaining clear communication with cross-functional teams. Provide training and technical guidance to new and junior staff. Act as a subject matter expert (SME) for complex procedures and ensure best practices are followed. You will provide support for colony maintenance. Ensure that special requirements are clearly labeled and supplied. You will be required to Interpret genotyping data, enter results in the database and develop mating schemes. This position will also involve other administrative duties including, maintaining and updating study-specific documentation and Standard Operating Procedures (SOPs). Develop new SOPs as necessary and ensure current procedures align with regulatory and operational requirements. All procedures must be documented appropriately and in compliance 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. All responsibilities are expected to be performed with minimal instruction, and you are expected to independently perform duties as described.
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Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree