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With a keen eye for detail and proficiency in relevant data management tools, you will contribute to the success of our clinical trial by maintaining robust data management processes and supporting the broader research objectives.
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Reporting to Dr David Levine, the Data Scientist will work across all phases of the research project, including extraction and organization of clinical and other data from a variety of information systems, automated data cleaning and verification, design, administration and construction of databases, analysis using valid statistical approaches, and development of new informatics and clinical tools.
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Clinical Research Data Scientist - (Boston, Rochester or Remote)We are seeking a highly skilled and motivated Data Scientist to join our Clinical Research team.
$125,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Performs scientific research, scientific writing and editing, including the writing and editing of project products to established government standards for the targeted science and lay audiences, proofreading of draft and final documents.
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We are using models early to fail less often, executing clinical trials to add valuation to the company, and generating fit-for-purpose data to feed back into Valo’s Opal Computational Platform as we reinvent drug discovery and development from the ground up.
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Profound knowledge of international guidelines (ICH-GCP) for the conduct of clinical research projects and experience with Clinical Database Systems and processes. Natural / life sciences or scientific background (university degree) or former experience in a CRO/ biotechnology/ pharmaceutical company in a Clinical Data Management position.
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Exciting contract Data Operations Manager opportunity available with a world leader in clinical research. Research/clinical trial experience. Electronic data captures (EDC) solutions, e.g., REDCap, Encapsia, Oracle Clinical, Medidata Rave.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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At least three years of experience, including: Research/clinical trial experience, electronic data captures (EDC) solutions, e.g., REDCap, Oracle Clinical, Familiarity with pharmaceutical informatics standards like CDISC and MedDRA.
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