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Certified Professional in Healthcare Quality (CPHQ), Master of Health Administration (MHA), Master of Public Health (MPH), or Project Management Program (PMP) or Lean/Six Sigma (Green or Black Belt) certification preferred.
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Our department also offers graduate degrees in Master of Athletic Training, Doctor of Physical Therapy, Doctor of Occupational Therapy, Master of Nutrition Sciences and PhD in Health and Rehabilitation Sciences.
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Mainframe Databases and File Systems: You need to know of these mainframe databases and file systems and have worked with at least one: DB2, IDMS, VSAM, IMS, Datacom, Adabas. Excellent written and verbal communication skills; including handling challenging Client or Associate Communications in high-pressure situations.
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A minimum of six years' experience in providing complex consultative services in the following focus areas: information strategy, big data architecture, information/data governance, master data management, data quality, data integration particularly in a life science or healthcare setting.
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Ensure that CDM documentation is filed into the Trial Master File (TMF) according to SOPs and the study plans; review CDM files for completeness and accuracy. Familiarity with clinical trial design and analysis activities and basic knowledge of regulatory guidelines (FDA/CFR, ICH/GCP.
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Occasionally a company will reach out for an in person focus group or clinical trial. If you're not comfortable using a webcam within a group study you can always pass and choose a different research study.
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Job Overview: Seeking a Clinical Research Scientist with strong expertise in Oncology, Immunology, or Immuno-oncology to lead the implementation, planning, and execution of clinical trial activities, collaborating with various stakeholders and driving Clinical Development strategy in a fast-paced, collaborative environment.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Experience with data integration tools (e.g., Informatica, Talend, Alteryx, SSIS etc) to carry out an ETL (Extract, Transform & Load) to move data from disparate systems to Master Data Management Hub.
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Position number : K0056207 Location of Employment : 11 th Judicial District, Cherokee County, Kansas 66725 Salary and Benefits : Trial Court Clerk II, Grade 18, $17.26 hourly Kansas Judicial Branch Benefits State Employment Center - Benefits (ks.gov) Job duties : Work involves general clerical duties in the Office of the Clerk of the District Court.
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Silberman offers seven degree programs: Bachelor of Science (BS); Master of Business Administration ( MBA ); Master of Business Administration – Management for Executives ( EMBA ); Master of Science – Accounting (MS-Acct); Master of Science – Taxation (MS-Tax); Master of Science – Supply Chain Management (MS- SCM ), and Master of Science – Digital Marketing (MS-DM.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Agile Scrum Master Certification or Agile Leader Certification. Minimum of two IT development programs as Agile Scrum Master. Release Train Engineer/Agile Coach. Agile Scrum Master Certification or Agile Leader Certification.
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Performs preventative maintenance (planned internal inspections) on equipment and completes required documentation and check-out file records. Strong knowledge of native plants, ornamental flowers, and/or urban agriculture with a focus on colorful annual planting.
$35.29 an hourExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Required Skills Master of Arts (MA) or Master of Science (MS) degree in archaeology or anthropology or related discipline. Required Experience Master of Arts (MA) or Master of Science (MS) degree in archaeology or anthropology or related discipline.
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Develop Master Production Schedule (MPS) and load into Jabils ERP system, including Purchase Order (PO) coverage. The Master Planner would own the build schedule, corrections and resolution of MPS to customer demand, planned tactics on deadlines for assemblies out of the various work areas on the floor, deadline for last shipment, and support plan for potential RMAs.
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Review and file necessary vendor laboratory documents for the Trial Master File (TMF) as applicable. 1-2 years clinical research central laboratory management experience or Biosample Operations experience.
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trial master file jobs Title: clinical research associate Company: Parexel
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