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5+ years of related experience, including 3 years of relevant industry experience, preferably in data services (data management and biometrics) or a clinical research environment. Knowledge of and experience in selling biometrics, regulatory submissions, and regulatory operations will be a distinct advantage.
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This position is primarily remote, non-office based, with the expectation to travel up to 50%. Understands the life sciences industry (e.g., CROs, pharma/biotech, medical device), scientific & clinical data/terminology, and the drug development process.
ExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges.
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This role will cover our San Francisco, California and Pacific Northwest up to British Columbia, Canada territory. Excellent skills using Microsoft Office Suite: MS PowerPoint, MS Word, and MS Excel. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating.
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Lead capabilities meetings and bid presentations comprising all aspects of MMS services and solutions. Territory management: actively prospect and leverage potential new business opportunities within specified customer accounts.
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The faculty have diverse teaching, research, service, and outreach expertise in the disciplines of forest biology and watershed management; forest economics, management, and policy; and forest measurements, biometrics, and spatial technologies.
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Provide high level and complex scientific and clinical guidance to Clinical Trials Management, Biometrics, Global Drug Safety, Regulatory and Project Management staff to meet project deliverables and timelines.
$250,000 - $340,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Provide statistical programming and validation support for clinical study reports and help coordinate programming activities with Biometrics lead and other study programmers to meet timelines. This position will work closely with the Director of Statistical Programming and other members of the Biometrics team to provide programming support across specific programs.
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Partner with EVA in using RWD to identify burden of disease, patient subgroups, endpoint validation and other health economic and outcomes research analyses to understand where new therapies may add value.
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Coordinate with other organizations including, but not limited to, Data Forensics and Biometrics Agency (DFBA), National Ground Intelligence Center (NGIC), Naval Criminal Investigative Service (NCIS), and FBI Special Investigative Unit (SIU.
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Provide expertise to provide support in all facets of I2 analysis, including, but not limited to, triage, research, exploitation, analysis, production, and dissemination of Biometric, Forensic, Face & Image Analysis, Cellular Exploitation (CELLEX), Document and Media Exploitation (DOMEX) derived products, and I2 training.
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In collaboration with clinical and project teams of the company, the successful candidate plans, designs, and executes clinical development research studies to evaluate the efficacy, safety, clinical pharmacology, and pharmacokinetics of biologic and cellular immunotherapies.
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It is made up of outstanding professionals in functions related to clinical research, including but not limited to biometrics, clinical operations, clinical pharmacology, medical science, medical writing, project leadership, project management, and regulatory affairs.
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Robust clinical research experience within the pharmaceutical/biotech industry. Track record of successful and emerging research in therapeutic areas relevant to Intellia’s development programs and pipeline.
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The High Tech Corridor is anchored on the north by Morgantown, which is the home of West Virginia University, a Carnegie Foundation Research Institution and training academy for Cisco systems, Inc. and Oracle.
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