- Merck & Co. (Durham, NC)
- …the globe.Reporting to the Director of Quality Systems and Compliance, the Associate Director - Quality Systems position will provide leadership, focus and ... these site-wide management programs by defining requirements established via in-depth review of existing systems and aligned with strategic direction defined by… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Vice President (AVP) will be responsible for leading the Translational Medicine (TMed) Cardiovascular & Respiratory Therapeutic Area and ... include the clinical pharmacology support of the Common Technical Document (CTD) and label, including relevant compound/program life-cycle management.The successful… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …post trial information on required public forums (eg.clinicaltrials.gov).- Under supervision, review and document CRO-generated reports, such as site monitoring ... the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the...Plan (CSOP).Responsibilities Prior TMF experience required!- Reconcile the TMF document trackers generated by the CRO with the … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. Summary The Associate Director of Regulatory Writing is a key role responsible for producing ... provide scientific and strategic insights at the study team level. The Associate Director of Regulatory Writing must possess advanced knowledge of BLA/MAA… more
- Genmab (Plainsboro, NJ)
- …and utilized at a pace never seen before. Join Genmab as an Associate Director, Solution Architecture and Engineering, R&D Digital Products as part of our ... and Development.Conduct current-state analysis, gap analysis, capability analysis, and document reference architecture for various R&D systems and functions.Provide… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …in design and geographic scope). Prepares clinical section of regulatory document . Collaborates as team member with AROs/CROs. Drafts development plans, protocol ... Leads dose-escalation meetings; Performs quality assessment with Delivery Lead eg review Tables/Listings/Graphs before database lock and quality check of data; Works… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …disorders. Responsibilities:- Protocol Development, Case Report Form (CRF; review ), Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, ... for complex studies including study design, protocol development, CRF review , SAP development, analysis files development, statistical analysis accuracy validation,… more
- Genmab (Plainsboro, NJ)
- …to fulfilling our purpose.The RoleThe Global Regulatory Labeling Strategy Sr Manager/ Associate Director will be responsible for leading the development and ... as relevant to support optimized labeling. Ensure proper development, review , approval, implementation, maintenance, distribution and tracking of labeling documents… more
- Merck & Co. (Rahway, NJ)
- …electronic prosecution documents are properly named and saved in the IP Group's document management system Review contents of patent application files to check ... certificates of correction) and prepare applications and other documents for filing- Review notice of allowance and file history; prepare documents for internal… more
- Insight Global (Waterloo, IA)
- Job Description The Document Review Associate performs Document Review according to standard procedures or instructions. Responsible for researching ... to a checklist. This person will receive almost 2 weeks of training to eventually review 150-160 documents a day. There will be project based work across the site… more
- J&J Family of Companies (Titusville, NJ)
- Johnson & Johnson Innovative Medicine is recruiting for an Associate Director Document Publishing. This position can be located in the US (Spring House, PA; ... potential. At Johnson & Johnson, we all belong. The Associate Director drives decisions impacting document processing,...the development and maintenance of processes and procedures for document preparation, review , and approval. + Ensures… more
- CBRE (Columbus, OH)
- Associate Project Manager ( Document Control) Job ID 185956 Posted 21-Oct-2024 Service line GWS Segment Role type Full-time Areas of Interest Construction, ... Columbus - Ohio - United States of America **About the role** The Document Control Coordinator, ("DCC") shall support CBRE's client with the implementation of the… more
- SitusAMC (Houston, TX)
- …require interactions across functions. This role will work directly with VP, Document Control with the document management activities across CRE ... operations/portfolios. This role will ensure the established document control process is being adhered to across the...compliance with company standards and procedures + Prepare, track, review , and enter data into data management system +… more
- NJM Insurance (Trenton, NJ)
- …Manufacturers (NJM), a top-rated insurance company, we are seeking a Mail & Document Processor, Associate in our West Trenton office.This role does require ... working in the office. The Mail & Document Processor, Associate is responsible for, but...regard to the timeliness, accuracy, availability, validation and quality review of scanned documents; is responsible for preparing incoming… more
- Actalent (St. Paul, MN)
- Seeking a Document Control AssociateKey Responsibilities: + Process, track, and manage QA documentation, including login, review , approval, distribution, and ... archiving. + Support the revision, review , and controlled distribution of Standard Operating Procedures (SOPs) and other cGMP-related documents. + Help resolve minor… more
- El Paso County (Colorado Springs, CO)
- Associate Engineer/Engineer/Senior Engineer (Development Review ) Print (https://www.governmentjobs.com/careers/elpasocountyco/jobs/newprint/4790792) Apply ... Associate Engineer/Engineer/Senior Engineer (Development Review ) Salary See Position Description Location Colorado Springs, CO...the department/office and the particular assignment. Changes to this document may only be made by a member of… more
- CTG (Oneonta, NY)
- …update and revise processes and procedures. + Support the management of the document review and retention processes. + Assist in continuous improvement ... exciting opportunity! CTG's premier client has a contract assignment for a ** Document Control Specialist** . **Type:** Contract **Job Title:** Document Control… more
- CTG (Buffalo, NY)
- …+ Complete additional duties as assigned. **Scope of Responsibilities** : + Perform document review according to established procedures. + Ensure accurate data ... Document Custody tracking system to original documents. + Review uploaded data in the tracking system to ensure...No supervisory responsibilities. **Education and Experience Required** : + Associate 's degree, **OR** + A combined minimum of 2… more
- Tutor Perini (White Plains, NY)
- ** Document Control Manager - Kensico-Eastview Tunnel Project** Office or Project Location **White Plains, NY** Company **Frontier-Kemper Constructors, Inc.** Job ... Code **2549** Frontier-Kemper, a Tutor Perini Company, is seekinga ** Document Control Manager** to join our Kensico-Eastview Connection Tunnel Project in White… more
- Fujifilm (Research Triangle Park, NC)
- …+ May have some assigned project responsibilities, such as department representation, document development or review , troubleshooting, and protocol execution. + ... **Overview** The **QC Lead Associate , Data Reviewer** position is a position that...within the Quality Control laboratory. The individual performs data review for testing of high throughput, right-first-time laboratory work… more
