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The key functions of this role will be to collaborate with internal and external stakeholders including the Foster City Medical Affairs team, Scientific Publications, Medical Affairs Research, Marketing, Global Commercial Product Strategy, Value and Market Access, Clinical Research, Public Affairs, Government Affairs, Contracts/Finance, Pharmacology, Virology and Legal on both the global and regional levels.
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In this function, the candidate will be translating pre-clinical /research methods and data to develop cGMP compliant processes and clinical drug product specifications, manage the execution of CMC studies and author drug substance/product IND sections.
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To work collaboratively on multi-functional projects and interact with biomarker scientists and scientists from other functions including clinical pharmacology, biology, bioinformatics, clinical research, and clinical data science on a regular basis.
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Qualifications:· Candidates should have a doctoral degree in bioinformatics, computational biology, statistics, data science, other relevant fields with at least 1-3 years/ master’s degree with at least 5-7 years/BS degree with at least 10 years of relevant post-degree experience, preferably in pharma/biotech or related research organizations/academia.
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Cell Solution’s vertically integrated solutions support preclinical research, clinical studies from phases 1 to 3, and commercialization with high-quality RUO and GMP-compliant starting material and apheresis collections.
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Support multiple projects simultaneously and work cross-functionally with colleagues in the oncology, chemistry, protein engineering, pathobiology, DMPK, biomarker, and clinical groups. Gilead Sciences (Foster City, CA) is seeking a talented and highly motivated Research Scientist/ Senior Associate Scientist to join our oncology research group.
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You will deploy and deliver technical solutions at the intersection of computational chemistry and machine learning, supporting research directions in molecular design across broader gRED and Roche.
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Nonclinical Scientific Writer-BioanalyticsDo you want to be part of an inclusive team that works to develop innovative therapies for patients?
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In addition, the incumbent is the key contact for Clinical Data Management, Research & Development Information Technology (RDIT), Statistical Sciences and Programming (SSP), Global Clinical Trial Management (GCTM), Global Site Management Operations (GSMO), Global Patient Safety & Epidemiology (GPSE), Clinical Development, and Non‐Translational Sciences (NTS.
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PharmD or PhD in pharmaceutical sciences, pharmacology or related discipline with 2+ years’ relevant research or clinical experience in the biopharma industry, healthcare, consulting, academia or a related environment.
$230,230 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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5+ years of experience in clinical science, clinical research, or equivalent. Proficient knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations.
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Clinical expertise and technical proficiency in administering Travel X-Ray Tech. Clinical expertise and technical proficiency in administering Travel X-Ray Tech. Stay current with new techniques, technology, and medications related to X-Ray Tech practice.
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AND or ASN (Associate Degree in Nursing/Associate of Science in Nursing Degree)BSN (Bachelor’s in Nursing) preferredCurrent Licensed Master Social Worker (LMSW)ASW (Associate Social Worker)Bachelor’s Degree in Social Work preferredLicensed Clinical Social Worker (LCSW) or MSW (Master’s Degree in Social Work) - years’ experience in clinical medical record auditing or equivalent role.
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Synthego’s mission is to enable agile life science research and development from discovery through clinical trials by providing scientists with comprehensive CRISPR solutions for each phase coupled with full technical and regulatory support from industry-leading experts.
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Duration: 12 monthsLocation: South San Francisco, CAAs a Scientific Researcher I, you will be:Job Description:The Scientific Researcher performs laboratory-based activities and processes related to the tracking registration inventory preparation e.g. DNA/RNA extractions from human biospecimens fluid and tissue samples human cell culture organoid culture Serum Plasma and PBMC isolation from blood samples and distribution of biological samples from clinical and non-clinical trials.
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clinical research affairs jobs Company: Biophase in Burlingame, CA
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