- Merck & Co. (Rahway, NJ)
- …and program cost estimates requested by Product Development Teams.-Responsible for authoring clinical supply documentation in support of labeling and packaging ... approach to identify process inefficiencies, develop solutions, and drive continuous improvement initiatives within the clinical supply planning function. -… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Job Summary: The Director of Data Management (DM) Reporting provides leadership in Data Management ... and external stakeholders to oversee the development and delivery of clinical data programming, reporting, data visualizations, external data acquisition and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. SummaryThe Sr. Director , Data Quality and Integrity (Global R&D & PV QA) ensures high ... process improvements. Collaborating with the Global QMS eCompliance team, the director oversees QA plans, promotes data governance, and engages stakeholders to… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Summary: The Associate Director , Laboratory Data Management is accountable for the end-to-end delivery of ... laboratory data in Daiichi Sankyo R&D collaborating with clinical and medical teams, clinical safety and pharmacovigilance, CROs and other vendors to ensure high… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …in? Are you ready to experiment with us? The Position The Director , Market Intelligence and Portfolio Insights will leverage Competitive Intelligence methodologies ... to provide key insights into the biopharmaceutical landscape across clinical , commercial, and enterprise domains. This role involves applying data interpretation and… more
- Formation Bio (New York, NY)
- …than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of ... processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma… more
- Formation Bio (New York, NY)
- …than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of ... processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Operations, including but not limited to - Commercial, Patient Services, CMR ( Clinical , Medical, Regulatory), Finance, and Novo Nordisk global colleagues, to deliver ... in fast-paced environments with a focus on quality and documentation .Skilled in change management and guiding teams through transitions.Excellent communication… more
- Henry Ford Health System (Troy, MI)
- *The Director Revenue Cycle Inpatient Clinical Documentation Improvement & Payer Audit is a Local Southeastern, MI role with flexible Hybrid opportunity ... we are seeking a highly skilled and experienced Clinical Documentation Improvement (CDI) Program Director to provide concentrated daily oversight of… more
- AdventHealth (Maitland, FL)
- …the strategic and operational planning, design, implementation, and oversight of the Clinical Documentation Improvement (CDI) program at Florida Hospital. ... Days **Location:** Orlando Florida **The role you'll contribute:** The Director - Clinical Document Improvement ...for recruiting and providing support, guidance and mentorship to Clinical Documentation Improvement team to… more
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