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Review/approve creation/modifications to Master Stability Protocols (MSP) and Study-Specific Protocols (SSP), batch-specific enrollment documentation, and LIMS stability studies. Use computer software/programs: Microsoft Office applications, SAP, LIMS, Quality Management System (e.g. Track Wise or Veeva), JMP, etc.
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Clinical partners include Robert Wood Johnson University Hospital in New Brunswick, University Hospital in Newark, and other affiliates. Aligned with Rutgers University-New Brunswick and collaborating university wide, RBHS includes eight schools, a behavioral health network, and six centers and institutes that focus on cancer treatment and research, neuroscience, clinical and translational research, advanced biotechnology and medicine, environmental and occupational health, and health care policy and aging research.
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Use computer software/programs: Microsoft Office applications, SAP, LIMS, Quality Management System ( TrackWise or Veeva), JMP, etc. Good organization skills and keen attention to detail Qualifications: (MS) or BS degree required with relevant cGMP experience in biopharma within a pharmaceutical manufacturing facility.
$64.15 - $69Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Responsibilities involve interacting with global and local IT support functions to define laboratory user requirements and master data to assist with the development and deployment of IT systems such as LIMS/LES (LabVantage, MODA), Electronic Laboratory Notebooks (NuGenesis), and other laboratory systems (Empower, WinKQCL, and others.
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The new collaboration also aligns RWJBarnabas Health with Rutgers’ education, research, and clinical activities, including those at the and. This unique role promotes mentorship and career growth potential by offering the opportunity to work as partners with other Department of Otolaryngology – Head and Neck Surgery faculty of the Rutgers Robert Wood Johnson Medical School.
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Provide inputs to different documents (e.g. trial protocols, amendments and plans; clinical trial reports; eCRFs/CRFs;TMFs) based on review. Minimum requirement: 12+ years experience in in drug safety/pharmacovigilance in clinical development and post-marketing preferably in oncology.
$170,625 - $284,375 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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From FX and CFDs to precious metals, master an exciting world of wealth management tools. Technology Ecosystem: Front-End: Power BI and SSASBack End: SQL Server and SSISArchitect: DataWarehouse and LakehouseCloud: Databricks with Azure Responsibilities Participate in ad hoc request where SQL queries needs to be written to pull data and ensure data is accurate.
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Trial experience, with a track record of success in the courtroom. Draft and file legal documents necessary for personal injury cases, including complaints, pleadings, and motions. Prepare and present cases for trial, including selecting jurors, arguing motions, meeting with judges, and presenting evidence.
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Certification in Lean, Six Sigma (Green Belt, Black Belt, or Master Black Belt preferred) Certification in Lean, Six Sigma (Green Belt, Black Belt, or Master Black Belt preferred) Lean/Six Sigma Implementation: Burlington, NJ Location.
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Cloud: Databricks with Azure. Front-End: Power BI and SSAS. Develop SSRS/Power BI reports as part of the small enhancement's requests. High level understanding of SSAS (SQL Server Analysis Services) Empower individual investors - and yourself - in the world of retail through a range of different financial products rooted in innovation and market intelligence.
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Must have Bioanalytical experience so they can help lab troubleshoot issues when applicable, Outsourcing experience preferred but the major focus/must haves should be at least 5 years (with masters or higher degree) or 10 years (with bachelors degree) bioanalytical experience, regulated experience, experience supporting clinical studies, biomarker ops or analysis.
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Access to our Clinical Nurse Liaison Team. Key Words: CT Technologist, CAT Scan Tech, Computerized Axial Tomography, CT Tech. MedPro Healthcare Staffing , a Joint Commission-certified staffing agency, is seeking a quality CT Tech for a contract with one of our top healthcare clients.
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Actively contribute to the development of regulatory strategies for investigational products in Investigational New Drug (IND)/ Clinical Trial Applications (CTA), Biologics Licensing Application (BLAs)/ Marketing Authorization Application (MAA), through evaluating scientific merits of Chemistry, Manufacturing and Control (CMC) and nonclinical study data package.
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In terms of plasmid service, GenScript ProBio supports the most clinical approvals for CGT drugs including mRNA vaccines, CAR-T in China. GenScript ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing.
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Maintain rebate vendor Master with Indirect procurement team. Provide Front office support after FSSC shift closure - Contract pricing and SAP SD transaction support for SAP V05 errors (Sales order) and VFX3 errors (Vistex Contract pricing.
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clinical trial master file jobs Title: trial master file in Somerset, NJ
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