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Principal Scientist Level: Ph. D. with 5+ years of experience or MS with 6-9 years of experience with degree in Pharmaceutics, Biochemistry, Chemistry, Pharmaceutical Chemistry, Molecular Biology, Bioengineering, Chemical Engineering or related disciplines.
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Established leadership skills, including management of individuals and teams working towards common clinical/scientific goalsConsistent track record of managing timelines and driving key results in a matrixed organizationExcellent communication, interpersonal, and written skillsPreferred Qualifications:R&D experience at a pharmaceutical company, biotech or partner organizationFamiliarity with drug discovery and clinical development processes.
$142,000 - $244,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Deliver impactful outcomes by leveraging a deep understanding and experience in navigating typical workflows within drug discovery, drug development, gene-to-antibody, and proteomics.
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Ph. D. in engineering, pharmaceutical science, chemistry, biochemistry, physics or other quantitative area of study with 0-3 years of experience; M.S in engineering, pharmaceutical science, chemistry, biochemistry, physics or other quantitative area of study with 3-5 years of experience; or B.S. in engineering, pharmaceutical science, chemistry, biochemistry, physics or other quantitative area of study with more than 5 years of experience.
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In-depth knowledge of analytical chemistry, with hands-on experience in chromatography techniques (HPLC, UPLC, 2D-LC) or electrophoretic techniques (CE-SDS, CZE, icIEF) for protein and nucleic acid analyses.
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Qualifications:PhD or MS in Analytical Chemistry, Chemistry, Biochemistry, or another relevant field. Overview Within the Translational Bioanalytical Sciences (TBS) group of Clinical Development, the role focuses on LC-MS/MS of small and large molecule quantitative assay development of biological samples.
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BMS is looking for a Principal Scientist with a desire to contribute in the fast-paced early development matrix environment by supporting pre-formulation, physico-chemical characterization, and formulation development of oral and parenteral dosage forms for new drug candidates in support of preclinical and clinical studies.
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Data Management and Analytics: Oversee the collection, integration, and analysis of large-scale scientific data sets, from the lab to the trials, utilizing advanced analytics and machine learning to extract valuable insights for drug discovery and development.
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Biotechnology, biological science, sterile environment, sample collection, Histology, Pathology, Ascp, Immunohistochemistry, Tissue samples, Chemistry, Biology, biochemistry, Staining, Accessioning, Specimen processing, Sample preparation, embedding, sectioning.
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Knowledge of quality control lab activities and procedures, technical knowledge of Analytical Chemistry. Or a doctorate from an accredited four-year college or University in chemistry, biochemistry, or a related scientific field with a preferred 1- 3 years of experience working in a laboratory in a manufacturing or academic setting.
$90,000 - $110,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Good theoretical understanding and experience in protein chemistry and biochemistry. Minimum B.S. degree in Analytical Chemistry, Biophysical/biochemical sciences, pharmaceutical sciences Or Master’s Degree in Biochemistry, Biotechnology, Biology.
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Demonstrated knowledge of principles of drug development, pharmacology, clinical trial methodology and design, medical monitoring of trials, assessment of drug risks and benefits, and safety assessment of drugs both on the market and in development and global safety regulations highly preferred.
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EXPERIENCE/EDUCATION: · B.S. in Science Field or related discipline is required (Chemistry or Bio Chemistry is preferred) · Knowledge in oligonucleotide synthesis and PCR technology is desirable · Knowledge in lab equipment automation and programming · Ability to work under cGMP guidelines, and coordinate/implement production schedule is necessary If interested, please share your updated resume at.
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Reporting to the Executive Director of Development Quality Assurance, the Senior Director of Pharmacovigilance QA serves as a strategic partner managing quality and regulatory compliance related to Good Pharmacovigilance Practices (GVP) and other related activities performed by Drug Safety & Pharmacovigilance and Medical/Clinical Departments.
$200,000 - $280,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The successful candidate excels in a collaborative, cross-functional, matrix team environment to enable the development of new drug products for pharmaceutics, biologics, and emerging modalities such as, but not limited to, antibody-drug conjugates, gene therapy, oligonucleotides, and SiRNA nanoparticulate delivery.
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chemistry drug discovery jobs in Piscataway, NJ
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