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The Senior Director will be the clinical lead to progress multiple early clinical assets from first-in-human through proof-of-concept and will prepare the clinical development plan, design clinical trials and lead the clinical development teams.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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In collaboration with medical director, Digital Medicine Lead, QS, and others, design study; execute on sensor-facing aspects of CES study, including liaison with vendor/device collaborator and User Experience Research (UXR.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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The Medical Director Clinical Programs is responsible for designing and implementing clinical programs with specific medical condition focus for all lines of business enterprise wide.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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With partnerships from other parts of Medical Affairs, Publications and Scientific Communications, Pharmacovigilance, Clinical Development, Market Access, and Commercial functions. The Director, Medical Research, is responsible for supporting strategic and operational activities of the Medical Affairs department and other functions at Intercept (e.g., R&D, Medical Safety) through real world evidence (RWE) generation.
$190,000 - $286,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This position requires candidate to have deep knowledge & advanced experience with SAS or R. This position is responsible of programming and data management under the direction of the Assoc Director/Director/ Sr Director Biostatistician/Statistician.
Full-timeExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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Leverage close collaborations with quantitative functions within CDS (e.g., Biostatistics, Bioinformatics), as well as in Clinical Research, Patient Safety, Medical Affairs, and Global Value and Access to anticipate and meet the evidence needs of regulators, payers, providers, and patients.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Partners with internal stakeholders including CSPV, Regulatory, Clinical, Medical Affairs, HEOR and other stakeholders to ensure expectations are clearly defined and met across participating teams.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Quality Monitoring: Screen and select Independent Radiology and Oncology physicians (readers) for assignment to studies based on indication specific BICR experience; regularly monitor reviewer metrics for quality control in support of clinical trial endpoint data, and collaborate with Imaging CRO on remediation efforts to ensure independent reviewer calibration; maintain database of readers for assignment to similar studies/indications.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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The Associate Director/Director, a member of Shionogi's Global Epidemiology and Real-World Evidence (GEE) team, is responsible for strategizing and generating real-world evidence using fit-for-purpose data to support global products at each stage of the product lifecycle.
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The Senior Director of Real-World Evidence Biostatistics plays a pivotal role in leading and overseeing the strategic direction and execution of statistical and real-world evidence initiatives within the organization.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Generate, within time, budget, and quality standards, real-world evidence including, but not limited to: natural history of disease, population characterization, assessment of treatment patterns and unmet need, development of external comparators, benchmarking of clinical outcomes, comparative safety and effectiveness research, and post-authorization studies.
$201,025 - $260,150 a yearFull-timeExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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In-depth knowledge of statistical methodologies, clinical trial design, and real-world evidence generation, with a focus on optimizing study design and data analysis. + PhD or MS (12+ years experience) in statistics or biostatistics or related scientific field with clinical trials, drug development, pharmaceutical industry or healthcare experience.
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Our client focuses on oral solid dose, including thermo and cold form blistering, bottling, cartooning, clinical packaging, stability packaging, specialized kitting, assembly, serialization, and secondary packaging.
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As a Digital Biomarker Lead reporting to Head of Digital Health Technologies you will be play a pivotal role in developing and incorporating digital biomarkers within clinical programs and revolutionizing clinical research at Regeneron.
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Solid Understanding of Clinical Terminology such as SNOMED, ICD9/10, CPT, HCPCS, READ Solid understanding of healthcare data, particularly electronic health records (EHR) and insurance claims, and experience working with healthcare data standards.
$201,025 - $260,150 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago
clinical director jobs in Morris Plains, NJ
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