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Serve as the subject matter expert on Veeva Vault and related clinical trial management systems (CTMS), electronic trial master file (eTMF), and regulatory document management systems. Expertise in Veeva Vault or similar clinical trial management systems (CTMS), electronic trial master file (eTMF), or regulatory document management systems.
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OR Master's degree in clinical laboratory science, medical technology or chemical, physical or biological science and 1 year training and experience in high-complexity testing; OR Doctoral degree in clinical laboratory science or chemical, physical or biological science with 1 year training and experience in high-complexity testing.
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This role is specifically focused on CMC partnerships in Cell and Gene Therapy in terms of process development, clinical and commercial manufacturing and will require a high level of engagement and collaboration.
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Health Care Professional degree required (e.g., RN/BSN/MSN, NP, PharmD) and 8+ years of pharmaceutical industry experience in drug safety & pharmacovigilance as a Safety Scientist for products in the clinical trial and post-marketing environments or MD with 4+years of clinical experience and 6+years of pharmaceutical industry experience in Safety Science, Clinical Development, or Clinical Research is preferred.
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To be considered for this position, applicants must be a licensed Massachusetts psychologist, specializing in clinical neuropsychology, who meets established professional training guidelines to practice as a neuropsychologist.
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As a key player in our team, the Associate Director of Clinical Pharmacology will play a vital role in developing and implementing nonclinical and clinical ADME strategies. 5+ years of experience for Associate Director or 8+ years for Director in clinical pharmacology, modeling & simulation, drug metabolism, and/or pharmacokinetics within pharma or biotech.
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Collaborate with clinical or nonclinical operations to develop appropriate laboratory manuals and assist with coordination of all bioanalysis activities. The Associate Director, Bioanalytical and Bioinformatics will provide scientific and technical leadership across Astria’s portfolio and be responsible for management and oversight of bioanalytical vendor relationships, supporting assay development and validation for our nonclinical and clinical programs.
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As a key member of the laboratory, you will support the execution of sample accessioning, management, and daily assay execution for a new automated high-throughput immunoassay program. Full Cycle Laboratory Processes: Manage and oversee full cycle laboratory processes, ensuring accuracy and efficiency in sample accessioning and assay execution.
$100,000 a yearFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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I'm working with a pre-clinical biotechnology company revolutionizing the field of antibody discovery through the integration of cutting-edge machine learning (ML) platforms. 8+ years of experience in antibody discovery and development, with a proven track record of advancing candidates to preclinical or clinical stages.
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The Associate Director of Biostatistics will closely collaborate with partner functions such as Medical, Clinical Research, Clinical Operation, Data Management, Statistical Programming, etc.
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Convene and provide manage project teams, which may consist of staff from the Office of Clinical Affairs and MassHealth with expertise in quality, data and analytics, and data management and/or staff from relevant vendors.
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Bachelors degree in Life Science (Biology, Molecular Biology, Biochemistry, etc.) + 5+ years of experience with genomics applications in an industry or academic research laboratory environment with demonstrated advanced theoretical knowledge of, and practical experience in Functional Genomics (CRISPR and other gene silencing) technologies and extensive understanding and experience in CRISPR protocols.
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Associate of Science Degree OR High School Diploma / GED and 1 year of related experience. Bi-Lingual/Spanish, Portuguese, Haitian Creole, or Cape Verdean Creole speaking preferred. The Mission of the Homeless Services Bureau is to improve the quality of life of Boston's homelessness citizens by providing emergency shelter, social services, and housing searching services.
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Manages the DFCI Biosafety Communications Program by identifying topics relevant to investigators with biosafety protocols such as upcoming modifications to IRIS for human gene therapy clinical trials and iRIS-IBC for laboratory registrations and any regulatory and DFCI policy updates, training requirements, resources and guidance, and those requested by the Director of Biosafety.
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Overview A Post-Doctoral Research Fellow position is available to join the Hill Laboratory in the Department of Medical Oncology at Dana-Farber Cancer Institute. We utilize immunofluorescence microscopy, cell and molecular biology, DNA damage repair, flow cytometry, and various sequencing assays on cell lines and patient-derived organoids to study DNA replication and cell cycle dynamics in different disease or pre-cancerous settings.
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clinical laboratory bachelors degree histology jobs Company: Northwell Health in Boston, MA
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