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Reporting to the Executive Director who oversees NonClinical Development and Clinical Pharmacology, the Director of Clinical Pharmacology will be mainly responsible to support pegozafermin clinical program.
$220,000 - $240,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Under the direction of the Pathologists and Laboratory Director/Manager, the Clinical Laboratory Scientist II performs all technical (including maintenance), analytical, clerical, and quality assurance tasks and duties associated with laboratory testing.
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As the Associate Director you will play a pivotal role in establishing and expanding the company's capabilities for preclinical in vitro and clinical ex vivo disease pathobiology. Experience with therapeutics programs that have yielded drugs entering clinical development in areas such as endocrinology, diabetes/obesity, immunology/inflammation, or metabolic disease.
$170,000 - $200,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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We are seeking an experienced and highly motivated Director/Senior Director, Drug Product/Formulation Development who will report to the VP of CMC. This individual will drive the drug product development and strategy including pre-formulation, formulation, scale-up and manufacture for all our preclinical and clinical projects.
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Works collaboratively with vendors, Clinical Research, Drug Safety, Regulatory Affairs, Clinical Operation, and Project Management teams to meet project deliverables and timelines for statistical data analysis and reporting.
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Based in South San Francisco, CA, and reporting to the Executive Director of Medical Affairs and Advocacy Engagement, this role will internally champion the patient voice, gather critical insights into the patient journey, and partner closely with Clinical, Communications, and other functions to develop a comprehensive Advocacy Engagement strategy.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Strong understanding of drug discovery and development processes, including preclinical, clinical, and regulatory requirements. Reporting to the Vice President of Portfolio and Alliance Management, the Senior Director will also contribute to portfolio strategy and decision-making processes to advance the company's pipeline and business objectives.
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In addition to duties as Residency Program Director, the selected candidate will also provide clinical services and direct supervision of residents in inpatient and/or outpatient settings.
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Reporting to the Executive Director, Process Development and Manufacturing, the Associate Director or Director, Process Development and Manufacturing is responsible for the design and execution of experiments to support process development and provides technical oversight of contract development and manufacturing organizations (CDMOs) for small molecule programs ranging from research phase to clinical development and eventually commercial production.
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These platforms are used by our lab biologists, chemists, and therapeutic area leads to orchestrate lab work, visualize and QC data across a growing array of modalities (imaging, RNA sequencing, proteomics, chemistry, etc), ingest and analyze in vivo and clinical datasets (sequencing, MRI, Histopath) from patient cohorts, and ultimately deliver data packages from our screening campaigns to inform our targets and therapeutics.
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Reporting into the Director, Clinical Operations the Clinical Project Associate will support the in-house day-to-day operational activities for the successful execution of a trial(s.
$87,000 - $104,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Medical Director is responsible for providing medical direction, management and review of clinical trials and product development. IDEAYA Biosciences (NASDAQ: IDYA) is a public, clinical-stage precision medicine oncology company committed to the discovery and development of targeted therapeutics for patient populations selected using DNA sequencing and other molecular diagnostics.
$271,493 - $299,327 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Director will primarily be involved in activities associated with the design, execution, monitoring, data interpretation, and reporting of clinical studies evaluating novel therapies across target indications.
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Understanding of the related disciplines (i.e. biostatistics, regulatory, pharmacology and toxicology research, cell therapy manufacturing, clinical pharmacology and pharmaceutical sciences) Reporting to the Head of Clinical Development, this individual will have oversight of and accountability for clinical trials from study start-up to BLA approval.
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Reporting to the Director of Clinical Operations and the Division Chair, the OFS Supervisor will be responsible for supervising services, staff and sychronization of the operational services for Pediatric Dentistry Clinics on Parnassus and Mission Bay.
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clinical director jobs in Daly City, CA
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