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Position Description:The Data Validation Specialist (DVS) validates Public Assistance (PA) grant applications for disaster recover projects in the completed lane with FEMA's PA delivery model. is looking to fill multiple full time Document Validation Specialists (DVS) to support a contract with the Federal Emergency Management Agency (FEMA) Public Assistance (PA) Program supporting FEMAs four Consolidated Resource Centers (CRC.
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O Investigate and document reports of non-compliance involving laboratory animal care and use, including preparation and submission of reports and other documents to the IACUC, IO, and regulatory and accrediting agencies when indicated.
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The IACUC Regulatory Compliance Specialist has the overall responsibility for ensuring regulatory compliance within the areas of the animal care and use program that fall under the responsibility of the IACUC office.
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Lead maintenance of ETF Capital Markets Policies, Procedures and any document retention. The ETF Capital Markets Specialist will contribute to the leadership of the ETF business at Natixis Investment Managers.
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Principal Duties and ResponsibilitiesResearch and document outcomes Research resources available for Medicaid adult/pediatric patients with behavioral health treatment needs, including but not limited to: outpatient individual or group therapy, psychiatry, partial hospital programs and inpatient programsUploads referral sources to, and maintains, resource SharePoint databaseSupport resource coordination around other patient service needs beyond behavioral health.
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Specialist Support: Consistent schedule that supports work-life balance Freedom to develop injury prevention plans Growth and development opportunities with the latest technologies, specializing in MSK Disorders In addition to a competitive compensation package with all the benefits you'd expect from an industry leader (401K matching program, insurance, paid time off, employee assistance, etc.
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Certification: Certified Registered Central Service Technician (CRCST) or Certified Instrument Specialist (CIS) preferred or certification required within 6 months hire : Computer skills, (Meditech, Instrument Management System preferred)SIGN ON BONUS: 3KA Physical Abilities Job Description is a component of this Job Description.
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Guides stakeholders through the CCC lifecycle, providing continuous education to internal and external partners on processes and the document review system, Veeva Vault. Reporting to the Manager of Marketing Operations for promotional review, the Specialist will be responsible for managing the Medical/Legal/Regulatory (MLR) review process.
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As a SOLIDWORKS Learning Experience Specialist, you will develop learning materials featuring Product Lifecycle Management (PLM) and Document Management software. Your primary responsibilities will include designing and creating self-paced eLearning materials or instructor-led materials that effectively challenge and engage a wide audience who use PLM and Document Management software.
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Manages document filing in the Trial Master File regulatory quality requirements. Significant understanding of regulatory requirements in preclinical and clinical study environment ideally for medical device studies (GCP, FDA, MDR, ICH, ISO, etc.
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As the Regulatory Affairs Operations Specialist, Ad/Promo, you will play a pivotal role in ensuring regulatory compliance and operational efficiency within our organization. Strong understanding of Regulatory Operations processes and systems including Regulatory Information Management & Document/ Data Management.
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IT Qualifications At least two of the following: PC/Laptop OEM Maintenance Certification CompTIA A+ Certification Microsoft Certified IT Professional (MCITP) certification in the desktop area Microsoft Office Specialist (MOS) Certification Experience in a similar role 3-5 years of relevant experience.
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Experience of project managing all technical elements of document review and disclosure matters, including database management, demonstrated by a track record of successfully managing multiple matters concurrently.
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Activities include all processes related to assuming and returning custody of customer documents, tracking and inventory control of source documents, document preparation, image acquisition, document indexing, image processing, and scanning images into appropriate systems/software.
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SOLIDWORKS PDM Administration Professional (CPAP) Knowledge of product data management (PDM) and product lifecycle management (PLM) applications. Benefits include a choice of plans providing comprehensive coverage for medical, dental, vision care for employee & dependents as well as employee life, short & long term disability, tuition reimbursement, immediate 401K enrollment, 401K match (50 cents on the dollar, up to the first 8% of your eligible compensation that you contribute based on match eligibility criteria), flexible time off policy, and 10 paid holidays.
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document specialist jobs in Cambridge, MA
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