Jobs at KCAS Bio

Execute regulated bioanalytical study activities, including sample preparation, extraction, LC-MS/MS analysis, data processing, and documentation. Troubleshoot routine assay and instrument issues, maintain sample integrity and chain of custody, support deviation investigations, and communicate study progress and risks. The role supports drug discovery, preclinical, and clinical studies involving drugs, metabolites, biomarkers, and endogenous compounds.

Leads biomarker ligand-binding assay development, optimization, troubleshooting, qualification, validation, and transfer. Designs experiments, evaluates assay performance, interprets complex scientific data, resolves technical issues, and supports PK and immunogenicity methods. Serves as a technical expert, mentors junior staff, collaborates with clients and quality teams, prepares study documentation, and ensures regulatory and quality compliance in a bioanalytical CRO environment.

Develops and grows business for bioanalytical and biomarker services across the Southeast United States. Responsibilities include prospecting, managing customer relationships, meeting sales targets, closing complex technical contracts, preparing proposals and Statements of Work, maintaining Salesforce and HubSpot records, and representing the company at conferences. The role requires expertise in regulated life sciences services, strong communication and selling skills, and 25–40% domestic travel. It is fully remote, with preference for candidates in the Southeast region.

Execute bioanalytical ligand binding assays supporting drug discovery, preclinical, and clinical studies. Responsibilities include sample and reagent preparation, assay execution, method development and validation support, data processing, troubleshooting, GLP-compliant documentation, sample tracking, and communicating study progress. The role requires increasing independence while providing informal guidance to junior staff.

Perform supervised bioanalytical studies using LC-MS/MS, including sample preparation, method development, analysis, data processing, troubleshooting, documentation, and sample tracking. The role supports drug discovery, preclinical, and clinical research involving drugs, metabolites, biomarkers, and endogenous compounds. Scientists will apply chromatographic and mass spectrometry principles, maintain regulatory compliance, communicate progress, and escalate issues to senior staff.

The Sr. Scientist in Mass Spec Development will lead bioanalytical projects, design experiments, conduct method development, and ensure compliance with study protocols and regulatory requirements.

Develop and grow strategic relationships across assigned life sciences key accounts, expand adoption of bioanalytical and biomarker services, achieve booking and revenue targets, manage account plans and pipelines, negotiate complex opportunities, and coordinate with scientific, operational, marketing, and program management teams. The role requires understanding CRO sales cycles, client pipelines, technical service offerings, and regulated bioanalytical environments.

The Director of Quality Assurance at KCAS Bio oversees QA departments, manages quality systems, leads regulatory audits, and interacts with executive management and clients to ensure compliance and high-quality standards in bioanalytical services.

As a Sr. Scientist at KCAS Bio, you will lead bioanalytical studies from setup to reporting, utilize your expertise in ligand binding assays, ensure compliance with GLP standards, and support client communications while mentoring junior scientists.