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Minimum QualificationsStrong Python coding to generate summaries and reports from standardized data setsExperience in clinical trial data quality assuranceExperience in clinical/health outcomes research, digital health technology assessmentMUST HAVE Experience in digital health, time series signals, physiological signals (ECG Experience, Sleep Signals, Blood Pressure etc.
$80 - $90 an hourFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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At least 8 years' experience and a, PhD, PharmD or MD degree with emphasis in clinical pharmacology, pharmacokinetics or a related scientific discipline. As a Director within the Clinical Pharmacology Group at Gilead, you will have significant responsibility and accountability for clinical pharmacology programs in Virology.
$221,170 - $286,220 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Clinical Trials Management Associate will work closely with Technical Operations to ensure drug product quality and delivery, Translational Sciences to ensure timely site biomarker sample collection and shipments, and support the clinical operations team with TMF filing and other duties as assigned.
$93,500 - $114,500 a yearFull-timeExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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Develop and integrate timelines and budgets for clinical pharmacology activities with overall company timelines and goals, in close coordination with project management, clinical science, CMC, DMPK, nonclinical development, regulatory affairs and other stakeholders.
$262,000 - $321,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Design, develop, validate, qualify, and implement clinical biomarker assays to support bioanalytical and clinical development of small molecule drug candidates. Experience with clinical assay development, validation, and qualification.
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The PV Clinical Associate leads clinical review of USDS cases (processed in-house or externally by the vendor) and supports the US Drug Safety PV Clinical Manager - Associate in all activities.
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Work with internal colleagues, offshore resources, and external vendors to ensure efficient, high-quality production of curated data for downstream use in sample tracking, production of statistical outputs for clinical study reports, biomarker analysis reports in support of Gilead's regulatory, scientific, and business objectives.
$130,220 - $168,520 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Licensed Clinical Drug and Alcohol Counselor (LCADC) is preferred. Preferred: Licensed Clinical Social Worker (LCSW), Licensed Psychologist (LP), Licensed ProfessionalCounselor (LPC), or Registered Nurse is required.
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The Senior Clinical Trial Physician, Rheumatology sits within Cell Therapy Clinical Development, which is a global organization dedicated to the effective design and execution of drug development.
$270,000 - $305,000 a yearFull-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Provides sample management expertise to the Study Management Teams (SMTs), Biomarker SubTeams (BSTs), and Clinical Pharmacology Subteams (CPST) FUNCTION: Clinical Operations – Biomarker and Bioanalytical Operations.
$86 - $90 an hourExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Proficiency with Medidata Rave EDC, Clinical Data Repositories and Visualization software. The Clinical Data Manager will be responsible for daily data management tasks for all phases of clinical trials including CRO/vendor oversight and support other functional areas such as clinical operations, statistical programming, and biostatistics.
$130,000 - $165,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Pyramid Consulting is seeking a local contract Clinical Lab Scientist (CLS) for a local contract job in Burlingame, California. Specialty: Clinical Lab Scientist (CLS) CERTIFICATION & LICENSURE CLSL-Licensed Clinical Lab Scientist.
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With a combination-focused pipeline that exploits the power of six scientific platforms (Immuno-Oncology, Tumor Drivers and Resistance, DNA Damage Response, Antibody-drug Conjugates, Cell Therapy and Epigenetics) to help address unmet clinical needs in a host of hematological cancers, we are motivated by a dedication to the scientific discovery and collaboration that will one day help eliminate cancer as a cause of death.
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Previous experience working in a matrixed environment to implement flow cytometry assay development and validation to support clinical trials. In this vital role you will design, develop and implement clinical biomarker assays employing innovative flow cytometry methods and techniques to support our drug development efforts.
$138,904 - $165,489 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Reporting to the Executive Director, CDM, the Senior Manager, CDM will be a highly motivated, quality-focused individual who can work collaboratively in a fast-paced, cross-functional team environment, and will oversee data management activities across multiple studies from study start-up through study closure in support of clinical trial objectives and corporate goals.
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Title: clinical Company: Arizona Western College in Burlingame, CA
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