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The Senior Research Scientist will assist in the development and maintenance of analytic datasets incorporating data from multiple sources including prospective cohort study data, clinical trials, and qualitative data, to develop and implement study designs while maintaining data quality assurance procedures to ensure validity and reliability of study results.
$150,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The primary responsibility of this Biologics Bioanalytical Research Associate is to provide bioanalytical support to DMPK project representatives on biologics discovery teams. Analyze, interpret, document and summarize biologics bioanalytical data.
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Research experience in statistics and computational genomics, and familiarity with next-generation sequencing data and analysis tools (preferred). Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it.
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Clinical Research, Study Documentation, Case Report File (CRF), ICF (Informed Consent Form), GCP, FDA, EDC, CTMS, Veeva, Medical Devices, SharePoint, Site Readiness, Site Qualification. The main function of the Associate Clinical Research Specialist, is to perform study start-up and conduct activities, ensuring clinical studies are conducted and reported in accordance with all applicable regulatory requirements.
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The Clinical Supervisor manages research project activities ensuring the quality and integrity of data collection, and trains, manages, and supports student staff and interns, reviewing work products to ensure study protocol is followed as written and approved by the institution’s IRB. This position will assist with the supervision of research coordinators.
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Under the broad direction of a Principal Scientist in ExQB, the candidate will support the execution of externalized In vitro projects across all discovery sites and our Research and Development Division's disease areas, as well as participate in relationship management of Contract Research Organizations (CRO.
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We are looking for candidates who are board certified/board eligible in Pediatrics, possess outstanding clinical skills, have experience in medical education or demonstrated scholarship and an ongoing commitment to research (e.g. clinical research, health services/outcomes research, community based participatory research or implementation science.
$210,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Develop, implement, and maintain quality assurance standards and practices, ensuring adherence to protocols, data integrity, and patient safety in all clinical research activities.
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Conduct biochemical research to assess the clinical and regulatory success of drugs. 2 years of experience understanding genetic mutations and their impact on the biological functionality of proteins, experience with genetic medicines including gene-therapy, gene-editing, cell therapy, mRNA and RNA silencing experience with pharmacokinetic, pharmacodynamics data and safety data.
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Build QSP models integrating biological, pharmacological, and physiological data to support drug development at all stages, from preclinical research to clinical trials and beyond, aiding in dose optimization, biomarker identification, safety and efficacy assessment, drug development decision-making, etc.
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Along with SRP or Clinical Leader and global development partners, responsible for oversight and high-quality implementation and closure of the study, ensuring data integrity. May act, in concert with senior clinical personnel, as the company spokesperson regarding publication of clinical research findings.
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The chosen candidate will be able to integrate processes across network serviceability, catalog management, audience segmentation, prospecting, order entry, payments, field management, provisioning, and data quality or augmentation.
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Proficiency in data analysis software used in LCMS (e.g., Xcalibur, Analyst). Requires extensive use of Microsoft Office (Word, Excel, and Powerpoint) and use of data analysis software Graphpad Prism, SoftmaxPro, and Phoenix WinNonlin.
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Join us in advancing cutting-edge clinical pharmacology research and contribute your expertise to our dynamic team! SystImmune Inc. is a dynamic clinical-stage bio-pharmaceutical company headquartered in Redmond, WA. Our mission is to revolutionize cancer treatment by developing breakthrough-therapeutic multi-specific antibodies and ADCs. With eight assets in ongoing clinical trials and a robust preclinical pipeline, we are committed to advancing innovative therapies from discovery through IND-enabling stages.
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Collaborate with different teams in EDM (Data Cloud, Architecture, Data Governance Tech, Data Science) and support strategic initiatives such as data governance, data-as-a-service, and self-service analytics.
$110,000 a yearFull-timeExpandApply NowActive JobUpdated Today
clinical research data quality jobs Company: Pwc in New York, NY
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