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Reporting to the Senior Director, Clinical Data Management, the Associate Director, Clinical Data Management will define and lead the clinical data management strategy for the organization.
$173,000 - $195,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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ASSOCIATE DIRECTOR CLINICAL DATA MANAGEMENT (This role is based in Company's Waltham, MA headquarters. The Associate Director, Clinical Data Management is responsible for overseeing the start-up and execution of multiple, complex trials with a CRO and supporting upcoming submissions.
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Working with Research Unit biology leads and Precision Medicine Companion Diagnostic leads to ensure alignment of preclinical, clinical biomarker and CDx strategies. Extensive experience in oncology translational research, with proven track record of high-impact contributions to biomarker discovery and implementation of biomarker strategy into clinical development.
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The Associate Director, Clinical Data Analyst, has a critical role in the delivery of high-quality external data across Dyne's development pipeline by proactively identifying, measuring, and mitigating risk prior to acquisition of non-electronic data capture (EDC) data.
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Assess: Comparative activity of novel biologics to research-grade control reagents or clinical- stage assets; reliability, repeatability and cost-effectiveness of assay systems. Alloy’s Translational Research team supports our drug discovery partners with in vitro and in vivo testing of therapeutic drug candidates across multiple modalities.
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Integrate clinical pharmacology knowledge with a broad understanding of and collaboration with related disciplines such as clinical development, biostats, regulatory, nonclinical, and research to support and impact development decisions.
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At least 5 years of clinical research experience at a pharmaceutical/biotech or CRO, with at least two years of clinical study management experience. The CTM reports to the Associate Director, Clinical Operations.
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The Clinical Scientist is a Director/Senior Director who will help design and execute the clinical development plan for Affinia’s cardiac and neurology gene therapy pipeline.
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Our solution integrates multi-omic molecular diagnostics with the latest cancer research and clinical information, performing sophisticated analytics to aid clinicians in selecting optimal personalized therapies.
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Visterra is a clinical stage biotechnology company committed to developing innovative antibody-based therapies for the treatment of patients with kidney diseases and other hard-to-treat diseases.
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Good understanding of US regulatory and compliance requirements for clinical research. Our client is a leading organization in the antibody driven Immuno-oncology space with a proven platform that has garnered multiple hundred-million dollar industry partnerships to drive their 5+ clinical trials.
$140,000 - $190,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Associate Medical Director provides specialist medical/scientific strategic and operational input into core medical affairs activities within their TA inclusive of healthcare professional/provider interactions; generation of clinical and scientific data; educational initiatives (medical education, data, guidelines and value proposition); safeguarding patient safety (risk minimization activities / safety surveillance activities.
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Collaborate with cross-functional teams, including Biology, Biologics, Clinical Operations, Clinical Development, and Regulatory Affairs functions, to align biomarker and CDx strategies with overall program objectives.
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Execute high throughput automated histology protocols (IHC, ISH) on animal and human tissues
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In addition to clinical responsibilities, the Medical Director will also be responsible for: supervising and evaluating all primary care providers and specialists, process improvement focused on clinical care, patient access, staffing, utilization management and patient scheduling, assisting in the development, implementation and monitoring of quality improvement and compliance efforts, budgeting and strategic planning.
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Title: director clinical research in Waltham, Troy, New York
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