- Elite Enterprise Resources (Albany, NY)
- …participation in the following activities: * Work with end users and/or review /analyze existing documentation or system artifacts to document business system ... requirements and processes, develop process models, and document requirements for the development/implementation of an exception tracking system for improved… more
- V2X (Columbia, MD)
- …and other government agencies as needed. Additional responsibilities include document control functions, personnel security actions, accountability of all ... operations. Responsibilities + Obtain information for Program Access Requests (PARs), review packages for accuracy, and proper routing. + Process customer's… more
- State of Colorado (Sterling, CO)
- …treatment program. This position will assist in the development and/or review of Substance Use Disorder therapeutic community treatment programs, provide Substance ... + Assist the outpatient treatment staff in delivery of services; + Document quality/compliance indicators, generating reports and presenting feedback to program and… more
- State of Colorado (Denver, CO)
- …compliance with state and federal regulations, conduct medication observations, and review nursing practices. You will also investigate serious incidents and ... complaints, determine whether agencies responded appropriately, and document findings in clear, defensible statements of deficiencies. This role requires a… more
- HSBC (Buffalo, NY)
- …The Mortgage Post Closing Specialist is responsible for a complete post-closing review , including but not limited to collateral review , disclosure ... reconciliation/remediation, receipt/ review of trailing documents and flood pre- review . Here's what you can expect: + Complete collateral (note) review for… more
- Sanofi Group (Cambridge, MA)
- …answers to IRBs and HA questions, protocol scientific and medical training, medical review of data within the scope of the Centralized monitoring, clinical and ... investigators + Develop the clinical part of Briefing regulatory documents, Common Technical Document for submission to regulatory bodies (FDA, EMA, PMDA etc ) and… more
- Sanofi Group (Morristown, NJ)
- …answers to IRBs and HA questions, protocol scientific and medical training, medical review of data within the scope of the Centralized monitoring, clinical and ... + Contribute to the clinical part of Common Technical Document for submission to regulatory bodies (FDA, EMA, PMDA...abbreviated protocol, the final protocol and protocol amendments + Develop/ review the Core Study Informed Consent Form (CSICF) +… more
- State of Massachusetts (MA)
- …and document observations with minimal supervision. * Perform technical review of design development and construction documents submittals, cost estimates, and ... and document observations with minimal supervision. * Provide technical review of plans, specifications, cost estimates, and related documents prepared by… more
- Arvinas (New Haven, CT)
- …will have a substantial role in the development of the clinical documents, the review of scientific and clinical data and the communication of data to the scientific ... this role include, but are not limited to: **Clinical Document Development** + Lead the development of clinical study...+ Contribute to the clinical portion of investigator brochures review for consistency and applicability + Contribute in the… more
- Commonwealth of Pennsylvania (PA)
- …Services (CJIS) compliance requirements. + A conditional offer of employment requires review of prior law enforcement employment records as required by Pennsylvania ... left. You will not be able to add a document to the application after it has been submitted....WORK BEHAVIOR 4 - TECHNICAL PAROLE AND CRIMINAL VIOLATIONS Review parole or probation cases for potential technical parole… more
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