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Document Preparation Jobs in Greensboro

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Search Results - Document Preparation Jobs in Greensboro
Law Firm Carolinas-Greensboro-
and court documents.  •  Support attorneys with document preparation, filing, and case management.  •  Maintain accurate electronic and paper client files and review documents for completeness.  •  Communicate professionally with attorneys, clients, courts...
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TEKsystems-Greensboro-
/analysis skills  •  Ability to work in a remote, contract environment  •  Proficiency in document preparation and reporting  •  Stakeholder management  •  Communication and briefing skills  •  Problem-solving and analytical thinking  •  Policy interpretation...
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WorkForce Unlimited-Winston Salem, 25 mi from Greensboro-
coordination, records management, supplier follow-up, and timely approvals. Key Responsibilities Support contract intake, document preparation, routing, and approval tracking for IDT Procurement. Maintain accurate contract trackers, action logs, renewal...
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Randstad-Lexington (NC), 32 mi from Greensboro-randstadusa.com-
multiple time zones.  •  Document preparation: prepare professional documents, presentations (powerpoint), reports, and correspondence, ensuring high accuracy and proper formatting.  •  Travel coordination: assist with booking and coordinating domestic...
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WorkForce Unlimited-Winston Salem, 25 mi from Greensboro-
coordination, records management, supplier follow-up, and timely approvals. Key Responsibilities Support contract intake, document preparation, routing, and approval tracking for IDT Procurement. Maintain accurate contract trackers, action logs, renewal...
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UNC Health-Chapel Hill (NC), 41 mi from Greensboro-appcast.io-
as needed.  •  Document Preparation: Write drafts of letters of support, faculty nominations, complex memoranda, and other high-level documents on behalf of the Chair and Vice Chairs.  •  Information Management: Organizes and maintains confidential electronic...
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SiteBridge Research, Inc.-Chapel Hill (NC), 41 mi from Greensboro-rippling-ats.com-
submission, site feasibility, ect.  •  Excellent working knowledge of FDA & ICH GCP regulations and guidelines is required  •  Experience with eSource, eRegulatory, and CTMS is required  •  Experience in study document preparation (CRF, eSource, logs, SOPs, etc...
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