Scientist 1
KCAS Bio
Scientist 1
KCAS Bio
GLP/GCP bioanalytical & biomarker CRO services
When you work as a Scientist I in the Flow Cytometry group at KCAS, you get to further our mission by applying your knowledge in bioanalytical and scientific principles to support study execution under the guidance of senior scientists. You will contribute to study activities from setup through data generation while building your foundation in assay performance, data integrity, and troubleshooting.
Our Flow Cytometry team utilizes advanced conventional and spectral flow cytometry instrumentation and analytical techniques to support bioanalytical testing in drug discovery, preclinical, and clinical studies, including immunophenotyping, cell-based assays, biomarker analysis, and functional cellular assays. Our scientists work with platforms including Cytek Aurora, BD Fortessa, and BD FACSymphony to develop and execute sophisticated multiparametric flow cytometry methods.
This role follows a structured Tuesday–Saturday work schedule to support ongoing study execution and operational needs. The hours are Tuesday - Friday, 11:00am - 8:00pm and Saturday, 9:00am - 6:00pm.
KCAS Bio is a full-service bioanalytical and biomarker contract research organization (CRO) that supports pharmaceutical, biotechnology, and academic clients by delivering GLP- and GCP-compliant development services for drugs, biologics, and cell/gene therapies. The company operates on a contract-based model, providing flexible, expert teams and scalable capacity to meet each project’s needs. Its workflow involves conducting bioanalytical assays and biomarker work within regulated frameworks, acting as an extension of clients’ laboratories to enable rapid, scientifically rigorous research. KCAS Bio differentiates itself through a collaborative culture, continuous learning, and a commitment to speed and adaptability, focusing on delivering high-quality results efficiently. The company’s goal is to help clients advance time-critical research and bring new therapies through development and regulatory stages quickly and confidently.
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