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Conduct internal audits to assess effectiveness of Entrada's GCP/GLP QMS and process compliance including Clinical Study Report (CSR) and Trial Master File (TMF) audits. BS in a scientific discipline, advanced degree preferred with at least 10 years of experience in pharmaceutical / biotech / clinical research industry with significant experience in GCP/GLP environment.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development.
$26 an hourExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Regulatory Knowledge: Experience working within a GxP (GLP/GMP) environment is essential. This includes understanding concepts such as protein structure and function, enzyme kinetics, molecular biology techniques, and cellular signaling pathways.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Can streamline research by delivering operational and cost efficiencies through the strategic insourcing of GMP, GLP and non-GLP research services from discovery through safety assessment.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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The candidate is also expected to support outsourcing efforts for designing, monitoring, execution and reporting of the nonclinical toxicology studies, have experience in managing regulatory-compliant toxicology studies in a CRO or biotechnology/pharmaceutical company, and have demonstrated understanding of GLP compliance and the relevant ICH & FDA guidance documents.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Experience with outsourcing and working with external academic and CRO partners to develop/transfer assays, oversee data generation/analysis and delivery of high-quality data from global clinical trials under regulated settings (GLP, GCP, GCLP and CAP/CLIA etc.
$143,500 - $205,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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AALAS certification at the Assistant Laboratory Animal Technician level (ALAT) or higher or ability to successfully achieve ALAT certification within one (1) year of hire/promotion required. You will be responsible for assisting in the training of animal care staff in the following; cage changing, microisolator cage changing techniques, autoclave/cagewash operations, and other husbandry duties.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Defines strategy for and oversees tactical execution strategic plan by direct reports to provide effective oversight of research, assay development in support of pre-clinical and clinical research, GLP animal studies, in vitro diagnostic development, and all R&D vendors.
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Scientific Knowledge: A strong foundation in discovery sciences and protein biochemistry is essential. Master’s degree in biochemistry, molecular biology, biotechnology, or a related scientific discipline with at least 5 years’ experience; Ph. D. preferred.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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This is a dynamic role participating in the advancement of preclinical research into the clinic, with particular focus on the execution of exploratory, pilot, and pivotal (GLP) toxicology studies.
Full-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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The Senior Scientist, Toxicologist will partner with the Vice President of Toxicology to develop and carry out the overall toxicology strategy for programs in both Discovery and Development. The Toxicologist will collaborate with external vendors, the internal preclinical pharmacology and toxicology team, and other stakeholders across the company to ensure efficient processes that scale with Verve's continued growth.
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Develop clear preclinical trial strategies, design and write non-GLP and GLP study protocols, monitor, document, and interpret clinical study data. Stay current with GLP and regulatory requirements to support preclinical submission regulatory submissions including INDs.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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The VP QA will direct all GxP Quality activities and ensures Aveo and its vendors are inspection ready, adhere to GLP, GCP, GPV, GDP and GMP applicable regulations, company policies & procedures.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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AVEO continues to develop FOTIVDA in immuno-oncology combinations in RCC and other indications, and has several other investigational programs in clinical development. AVEO currently markets FOTIVDA (tivozanib) in the U.S. for the treatment of adult patients with relapsed or refractory renal cell carcinoma (RCC) following two or more prior systemic therapies.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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This role will have a focus on auditing and Global Compliance support to R&D & GCP activities but also to the GMP manufacturing sites, GDP, PV, and GLP related functions. Knowledge of cGMP, GCP and GLP required.
ExpandApply NowActive JobUpdated 3 days ago
glp job Company: Genoskin in Lynn, MA
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