Document Management Salary at Albridge BETA

Who We Are: TransPerfect is the world's largest provider of language services and technology solutions for global business. From offices in over 120 cities on six continents, TransPerfect offers a full range of services in 170+ languages to clients worldwide. More than 5,000 global organizations employ TransPerfect's GlobalLink® technology to simplify management of multilingual content. TransPerfect has global headquarters in New York, with regional headquarters in London and Hong Kong. What You Will Be Doing: The Study Owner (SO) works on behalf of clients as an extension to their study team. The Study Owner ensures a complete, contemporaneous and accurate Trial Master File (TMF) and electronic TMF (eTMF) across our clients’ clinical programs. Working with client study teams and functional leads, they assume a key role in the management of a study with a focus on study start up and the TMF with the goal of supporting inspection readiness. Participate in client Study Owner engagements

About Us: At Cooper University Health Care, our commitment to providing extraordinary health care begins with our team. Our extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols. We have a commitment to its employees by providing competitive rates and compensation, a comprehensive employee benefits programs, attractive working conditions, and the chance to build and explore a career opportunity by offering professional development. Discover why Cooper University Health Care is the employer of choice in South Jersey. Short Description: The Training Document Management Specialist is responsible for documenting revenue cycle processes across the system and develop instructional training modules that includes videos, in classroom training, online training, virtual content training. Each module to include an end user assessment and pre and post training. This role wi

Reports to: Director, GMP Quality Assurance Location: Princeton, NJ (hybrid) This role is responsible for providing GMP QA expertise, oversight, and auditing support of contract manufacturing organizations of small molecule, oral dosage formulations. Additionally, this role supports PMV’s GxP procedures program, document control, and training activities, utilizing an electronic document management system. Responsibilities Support GMP QA activities spanning across CMC (Chemistry, Manufacturing & Controls) for drug substance, drug product, and clinical trial material, for all outsourced GMP activities. Ensure all API, drug product and packaged and labelled investigational material meet GMP regulations, as applicable to phase of development, and are released in a timely manner. Collaborate with CMC, Clinical Supplies Management, Regulatory Affairs, and other departments to resolve quality issues and implement process improvements. Review and approve GMP-related documents, including master

Job Description Client is seeking a detail-oriented and motivated Temporary Administrative Assistant to support their Personal Lines Service Teams. This part-time, temporary position involves a mix of remote and in-office work. The ideal candidate will be able to manage administrative tasks with precision, demonstrate strong attention to detail, and work independently with minimal supervision. Location: Remote: Mondays & Fridays In-Office: Tuesdays, Wednesdays, and Thursdays at Holman Insurance, Maple Shade Location Working Hours: 8:30 AM - 5:00 PM Part-time, 20-25 hours per week Roles & Responsibilities Key Responsibilities: Document Management: Retrieve documents from insurance carrier websites. Accurately enter documents into our Agency Management System. Ensure proper naming conventions and activity codes are utilized. Administrative Support: Assist the Supervisor with various administrative requests as needed. Data Entry and System Navigation: Enter data with high accuracy and att

Kindle Energy LLC (“Kindle”) specializes in the management, optimization, and development of power generation in the United States and Canada and is a portfolio company of Blackstone Inc. (“Blackstone”). Blackstone is a leading global alternative asset manager with $1 trillion of total assets under management. Currently, Kindle manages 8.7+ GWs of generation in Ohio, Indiana, and Louisiana, with a 700 MW CCGT project under construction in Louisiana and a 160 MW natural gas fired facility under construction in Colorado. Kindle is currently recruiting for the newly created role of Document Control Manager, a key role in our in-house legal team. The position is based in Princeton, NJ and will report to one of the members of our Princeton-based legal team and work closely with the entire company, with frequent exposure to the executive management team as well as cross-functional team members at Kindle. The position requires minimal (if any) travel. If you are passionate about documentation

Job Description Job Description *THIS IS NOT A REMOTE OR HYBRID POSITION* Responsibilities: Answering and transferring calls Managing bill payment Organize and maintain documents Biweekly payroll and tracking employee commission maintaining Assists in auditing clients’ files, tracking and organizing documents Managing CRM, client follow-ups, organizing client information, and maintaining accurate data related to clients Review loan applications for completeness Income calculation Provide loan officer with information regarding borrower’s files Work with third parties to obtain items such as title and HOI documents Maintain and manage the pipeline Run credit, order appraisals, and preparing required worksheets (i.e., fee worksheet, LE, etc..) Prepare and submit document requests Work with loan officer, investors, and all other parties to clear conditions Request funding confirmation on all borrower files Perform and opening items audit on all borrower files Communicate with borrowers ab

Ajilon - JobID: 092A6183-1F5C-4954-A1CD-2791FEACF43C [Administrative Assistant / Data Entry Clerk] As a Document Specialist at Ajilon, you'll: Sort and deliver mail, incoming checks and invoices; Scan in checks and documents via OnBase; Use scanning equipment to convert paper record documents to an electronic format; Index record number into document management software...Hiring Immediately >>

Legend Biotech is seeking QA, Document Control Specialist (1st Shift) as part of the Quality team based in Raritan, NJ. Role Overview The QA Document Control Specialist (1st shift) role is an exempt level position with responsibilities for supporting the document management process within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment. This role will ensure compliance within the document management system, document storage and retention, and document issuance and reconciliation. Key Responsibilities Serve as a Document Control reviewer for new and revised procedures and documents to ensure compliance with global and site procedures Support Document Management system users with workflow handling and electronic system usage Manage the periodic review process for procedures Issuance of batch related documentation in support of GMP manufacturing Reconcile GMP documentation following document lifecycle requirements Cre