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Strong knowledge of pharmacokinetics and pharmacodynamics principles, immunogenicity, modelling and simulation, Model-Informed Drug Development, ADME Concepts, and regulatory clinical pharmacology requirements to support clinical development and regulatory submission.
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Be a hero for our rare disease patients
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Ensure that clinical trials are executed according to the Clinical Development Plan (CDP), trial plans, OGSM and in compliance with argenx procedures, ICH-GCP and other applicable legislations.
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Meet regularly with your Regional Clinical Director. Care is at the center of everything we do at BHW. Our dedicated clinical team works directly with children, adolescents, families, and their network of professionals to achieve meaningful outcomes through evidence-based therapies and techniques.
$89,250 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The Clinical Education Account Manager (CEM) supports HuFriedyGroup's academic institutions business by delivering cutting edge research and education to thought leaders and clinicians within dental schools as well as dental hygiene and assisting programs.
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The Clinical Finance Office seeks a Dental Financial Coordinator to oversee the workflow of dental clinical finances related to state Medicaid/Medicare programs, including MassHealth and other identified programs administered by Dentaquest and Skygen/Scion.
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May simultaneously function as lead CDM for multiple clinical trials or oversee the data management across a program. Familiarity with clinical trial design and analysis activities and basic knowledge of regulatory guidelines (FDA/CFR, ICH/GCP.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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This person will work closely with the clinical project scientist team and Clinical Leader in Late Development, in collaboration with other functional disciplines, including GCO, Data Management, Statistics, Regulatory, QMMC, and GMS to ensure flawless and integrated execution of study start-up planning, oversight, and reporting of clinical studies in Oncology.
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And respond to regulatory inquiries related to DMPK, PK/PD, and clinical pharmacology. Ensure that appropriate PK, PD and PK/PD data analyses (including population PK, PK/PD modeling and simulation) are conducted for each study/program while adhering to timelines and budgets to insure prompt and accurate execution of deliverables from clinical pharmacology studies and programs.
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Prepares clinical conference presentations under direction of presenter as needed. May be responsible for scheduling numerous complex research protocols, involving extensive interaction with those associated with in-house studies, grant-funded studies and industry-sponsored clinical trials.
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Summary The Senior Clinical Compliance Auditor is responsible for developing, auditing plans, and collaborating with Operations and Revenue Cycle in auditing/monitoring compliance requirements across all Company business units and service lines.
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May include direct line management of Clinical Operations staff. Multi-dimensional Clinical Operations background with capability of devising plans for operational challenges such as site activation, subject enrollment, monitoring oversight, protocol deviation management, data cleaning, etc.
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The Hematology Clinical Research Group at the Dana-Farber/Boston Children’s Cancer and Blood Disorders Center is seeking a clinical research manager. The Dana-Farber/Boston Children’s Cancer and Blood Disorders Center has exceptional research and clinical programs in non-malignant hematology.
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As the fastest growing behavioral health practice group in the country, now is the perfect time to join our clinical team! We perform essential, yet non-billable clinical and administrative functions that comprise the infrastructure needed to maintain a successful, busy practice so that you can focus on your clinical work.
$100,000 - $135,000 a yearExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Strong familiarization with Good Clinical Practice (GCP) and drug development processes, ideally Phase 1 – 3; ideally paired with experience in Oncology / Immuno-Oncology. Perform high quality clinical data review and identify clinical data insights through ongoing patient level review and trends analysis, thereby supporting for example Interim Analysis, Database and Post Lock activities and resolution of scientific & medical issues throughout the study lifecycle.
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Title: clinical Company: F Hoffmann La Roche in Boston, MA
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