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Frontage Laboratories, Inc

Verified Job Source

Accelerating Discoveries, Transforming Lives!

Exton, PA

Research Services
501–1,000 people

About

Frontage Laboratories is a US-based Contract Research Organization (CRO) that was initially established in New Jersey in April 2001 and later relocated to Pennsylvania in 2004. As an FDA-registered and inspected global pharmaceutical development and manufacturing organization, Frontage is headquartered in Exton, PA, with a state-of-the-art 28 facilities spread across Pennsylvania, New Jersey, Illinois, Ohio, California, Florida, Canada, Italy, and China. We are dedicated to accelerating the development of innovative therapies by providing a broad range of science-driven and quality-focused services including drug discovery, DMPK, preclinical safety & toxicology, formulation development and manufacturing, analytical, clinical trials, bioanalytical, and central labs. Frontage has enabled many biotechnology companies and leading pharmaceutical companies of varying sizes to advance a myriad of molecules through development and file regulatory submissions in the US, EU, China, and other countries.

Open positions

Lab Assistant-Sample Coordinator & Archivist

On-site · Vancouver

The Lab Assistant is responsible for archiving study data, managing laboratory inventory, and ensuring all documentation complies with GLP standards. They also handle the receipt, labeling, and storage of samples while coordinating shipping and delivery schedules.

Research Assistant I

On-site · Vancouver

Perform laboratory procedures including cell culture, molecular extractions, and various assays while maintaining equipment and documentation. Ensure strict adherence to SOPs, safety protocols, and study report requirements.

Research Scientist

On-site · Vancouver

The Research Scientist will plan and execute in vitro and in vivo metabolism and bioanalysis assays while performing data analysis and interpretation. They will also participate in method development, prepare study protocols and reports, and coordinate with study teams to ensure regulatory compliance.