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Candidate will work in close partnership with the clinical biomarker, diagnostics, and bioanalytical sciences groups within BST. Work with study teams to develop clinical sample management plans, as well as review and contribute to clinical study protocols, informed consents, and central laboratory documents to ensure quality and accuracy.
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The Braintree office, south of Boston and located just off Route 3 within easy walking distance to the Braintree MBTA station, also offers Pediatric Urgent Care (after hours), Adult Primary Care, an assortment of surgical & medical specialties and on-site laboratory, pharmacy, and radiology services.
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Extensive experience in a biologics upstream process development laboratory. The incumbent will work remotely and collaboratively with internal stakeholders and be responsible for the process development, tech transfer, and oversight of engineering/clinical batches at contract manufacturing sites.
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Oversees the validation and integration of new diagnostic assays into the clinical flow cytometry laboratory framework, including measurable residual disease (MRD) monitoring, myelodysplastic syndrome (MDS) assessment, cell sorting for FISH and molecular applications, DNA ploidy, and flow cytometry-based functional assays.
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The Audit Management group conducts Good Clinical Practice (GCP), Good Laboratory Practices (GLP), Good Pharmacovigilance Practice (GVP) and Information Technology (IT) audits and qualifications.
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You will have familiarity with FDA regulations, GCP, essential studydocuments, and key study activities such as; tracking patient screening andenrollment, clinical laboratory sample collection, regulatory documents, andstudy team communications.
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This position provides preventative and clinical medicine services, disease diagnosis, clinical oversight and training for laboratory animal husbandry, and training and participation in experimental techniques for animals used in biomedical research and education at Boston University and its affiliates via the BU Animal Science Center (ASC.
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The Cytogenetic Technologist is also responsible for confirming accuracy of test results and reporting laboratory findings to the Clinical Director and other Clinicians. Preferred Qualifications:One year clinical laboratory experience.
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Bachelor’s degree in biological or chemical science or medical technology or clinical laboratory science. The individual in this position reports to the HLA lab Technical Director and is responsible for compliance, quality assurance and performance improvement, and assists in ensuring optimal laboratory operations.
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Other clinical duties may include facilitating in-home diagnostics, point-of-care testing, administration of medications and other treatments, remote patient monitoring, clinical documentation, drain management, wound management, interpretation of diagnostic imaging & laboratory data.
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Education: Associate’s degree in Medical Laboratory Technology, Clinical Laboratory Science, or a related field. Requirements Experience: Minimum of 1 year of experience in a clinical laboratory setting preferred.
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If you are passionate about chemical safety and waste management and have a strong track record of success in managing laboratory waste. At least 5 years of experience in laboratory waste management, chemical safety, and handling.
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Shift: 12:30PM - 9pm or 3PM - 11:30 PMMon-Friday rotating weekends Job Duties/Responsibilities:Responsibilities are interchangeable within job titles of medical laboratory scientist (MLS), medical technologist or clinical laboratory scientist.
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Flexibility to work overtime or other shifts depending on business needs Requirements:Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements.
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Specifically, this position will work to establish control strategies, specifications and testing & inspection procedures for raw materials used to manufacture clinical-stage gene and cell therapy products.
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clinical laboratory jobs in Jamaica Plain, MA
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