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Candidate has 5+ years of relevant experience in the pharmaceutical or biopharmaceutical industry; and, has a BS or BA. (1) PMP certification or equivalent certification, (2) Candidates can be current or former project managers & (3) Project management experience in Pharmaceutical or Healthcare industries.
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Perform protein purification, QC, and protein bank registration to support the preclinical development of biopharmaceutical programs across multiple therapeutic areas. Top 3 Nice to Have Skill Sets: Protein purification, Protein characterization, working knowledge of AKTA Avant/PURE.
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The In Vivo Pathology (IVP) team within the Pathobiology department is seeking a research associate to contribute to histology and pathology workflows in support of pre-clinical in vivo pharmacology studies.
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Conduct nonclinical development activities (pharmacology and toxicology) for IND-enablement of gene therapy products. Design, manage and conduct nonclinical hands-on studies (GLP and non-GLP) for inclusion in regulatory submissions, including pharmacology, toxicology, and biodistribution studies.
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Integrate the latest in cell culture techniques and analytical methods to increase throughput and information content in our in vitro screening and pharmacology. Juvena’s approach integrates proteomics, transcriptomics and imaging with phenotypic human in vitro disease model screening and extensive preclinical validation to mine stem cell secretomes as a rich source of new medicines for chronic and rare diseases.
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PhD in cell biology, immunology, pharmacology, molecular biology or a closely related field with 0- 3 years of industry experience or a B.S. with a minimum of 6 years of industry experience. Significant laboratory experience is required with the abilit y perform flow cytometry of primary murine and human cells, ELISA, and MSD.
$113,000 - $138,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Our basic investigative activities concentrate on immunology, genetics/genomics, pharmacology, DNA repair and oncogene action. Our basic investigative activities concentrate on immunology, genetics/genomics, pharmacology, DNA repair and oncogene action.
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The non-profit company is creating a first-of-its-kind cloud-based platform between the biopharmaceutical industry and health authorities worldwide. Sponsored by leading biopharmaceutical companies, Accumulus Synergy was formed in 2020 to create innovative solutions that can reduce regulatory review times and transform global data exchange.
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Experience in a commercial-stage pharmaceutical/biopharmaceutical, preferred. Publicly traded Peninsula biopharma firm seeks an Executive Director Accounting will be responsible for overseeing much of operational accounting, including internal controls, monthly close, ERP systems, treasury, insurance, payroll and stock administration, risk management and compliance, and policy development and implementation.
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Our client, a clinical-stage biopharmaceutical company, is looking for a (Sr.) Manager of SEC Reporting & Technical Accounting to join their growing team. Our client, a clinical-stage biopharmaceutical company, is looking for a (Sr.) Manager of SEC Reporting & Technical Accounting to join their growing team.
$140,000 - $185,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Support key functions such as Clinical Pharmacology, Biomarker Sciences, Clinical Operations, and Clinical Development on GCLP laboratory quality strategy. Understand the use and application of bioanalytical and biomarker assays in clinical trials.
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We want to hear from you if you have 1-4 years of patent prosecution law firm experience, patent bar membership, and a background in one of the following fields: cell or molecular biology, immunology, biochemistry, bioinformatics, organic chemistry, medicinal chemistry, cancer biology, pharmacology, biophysics, or digital health focused disciplines.
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Working knowledge of purification techniques including affinity, ion exchange, size exclusion, hydrophobic interaction chromatography using Akta Avant/Pure or BioRad NGC. currently has an exciting opportunity for a highly motivated research associate to join our protein purification and QC group within the Protein Therapeutics Department.
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Our client is seeking a highly motivated individual at the RA II or Sr. Research Associate level within the NDCP function (Non-clinical Development and Clinical Pharmacology). Perform in vitro ADME/DMPK assays, such as CYP inhibition, metabolic profiling, etc.
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Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Working knowledge of documents related to GMP and development regarding Manufacturing, Analytical Development and Supply Chain.
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pharmacology biopharmaceutical jobs in Foster City, CA
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