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Qualified Citizen Screw Set up Level Machinist will have exemplary manufacturing skills, a working knowledge and experience as a Citizen Type Swiss Programmer/Machinist. The Swiss Machinist Compensation range.
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We are actively seeking an experienced and dedicated CNC Programmer to join and grow in the PPG organization. Utilize advanced programming skills to operate 3-5 axis mills, lathes and mill/turn machines, including expertise in Hermle, Doosan and Okuma systems.
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Senior Rave Programmer Responsible for designing the eCRF in leading EDC systems in Rave. Sr. Clinical Programmer Analyst. Serve as system administrator to grant user access using iMedidata Cloud Administration for RAVE EDC, Coder, Lab Admin, RTSM and MMI (Imaging) provide Oversight, guidance, and design of study build activities on Rave URL.
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Insmed is seeking a Senior Research Associate with significant experience with droplet digital PCR (ddPCR). Excellent communication skills with ability to interact professionally with colleagues and present research results in written reports and team presentations.
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Minimum 10 years of relevant work experience to include data management and/or database programming and spec Design activities including 10 years in Medidata RAVE. Knowledge of clinical trial process and data management, CRF/eCRF Design, CDISC. Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies.
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The UCSF Department of Surgery is recruiting for a Clinical Research Nurse to manage several clinical trials in the Division of Transplant, with a primary focus on islet transplantation for treatment of diabetes.
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The CNC Programmer is responsible for creating and improving CNC programs for 3-4 axis lathes and vertical/horizontal/multi-axis machines under minimal supervision. 5 or more years of experience in CNC programming (Mastercam) and CNC machining.
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Provide technical support and troubleshooting for Rave study development as well as site management and user access within supported RAVE modules. Responsible for conducting Quality Control of study design for assigned projects and participate in the validation of EDC studies.
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Technical expertise, technical writing ability, and proficiency in Systems Development LifeCycle (SDLC) principles. Responsible for the preparation and /or review draft and final eCRF, edit check specifications for assigned projects to ensure quality and consistency.
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The contractor Research Associate will work closely with the Analytical Development team in the Tech Dev department to help methods development and test samples utilizing PCR, ELISA, Gel Electrophoresis, cell-based and other assays; as well as to contribute to design and performing experiments with supervision as needed; complete assigned tasks within time frames with high quality; maintain a well-documented record of activities in ELN and reports.
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The Role The Sr. Research Chemist will support new Chemical Mechanical Polishing/Planarization (CMP) slurry formulation development and provide chemistry/chemical component expert consultation to the technology development team.
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Knowledge of clinical trial process and data management, CRF/eCRF Design, CDISC. Insights into creating actionable dashboards and deep understanding and knowledge of good interpretation of clinical data.
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Demonstrate excellent problem-solving skills, a proactive approach and the ability to make sound decisions. 12 Months contract (Possible extension/conversion) Responsible for the creation and maintenance of library objects within the Global Libraries.
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Pay Grade/Pay Range: Minimum: $53,500 - Midpoint: $66,900 (Salaried E8) Department/Organization: 200722 - Center for Instructional Technology Normal Work Schedule: Monday - Friday 8:00am to 4:45pm Job Summary: The Audio Visual Programmer I provides application and system administration to multiple systems that provide required services to Audio Visual Solutions (Jamf Admin and Jamf Server, Adobe Admin, Smart Deploy Server, Deep Freeze Server, PDQ, Hypervisor Server, etc.
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Minimum of two (2) years experience coordinating research protocols OR (2) years experience in cancer research OR certification as a Certified Clinical Trial Investigator (CCTI), Certified Clinical Research Coordinator (CCRC), or Certified Clinical Research Professional (CCRP) from the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SoCRA.
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Title: research programmer Company: Sol Price School Of Public Policy
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