- Aequor (Seattle, WA)
- …communication - Experience working cross-functionally Position Summary: The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP ... Client Cell Therapy Above-site organization, including the document approvals, document change control process, periodic review and system reporting.… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …that fall under the responsibility of the R&D Procurement group. The Associate coordinates with R&D Procurement team members, Purchasing, Legal, Finance, vendors and ... needed.Responsibilities- Contract Coordination: Collate exhibits to create contract draft, Review contract documents for completeness and accuracy; Ensure compliant… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …post trial information on required public forums (eg.clinicaltrials.gov).- Under supervision, review and document CRO-generated reports, such as site monitoring ... clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good Clinical… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …compliance, and patient safety related to managing assigned clinical trials, document management and management of clinical trial management systems and archiving ... to: Management of clinical trial documents, including but not limited to document receipt, distribution, uploading, indexing, archiving and initial quality review… more
- Merck & Co. (Rahway, NJ)
- …job that provides both technical and project management responsibility. The Associate Specialist - Manufacturing Automation position will report to the Director, ... production, utility systems and associated infrastructure.- Responsibilities of the Associate Specialist - Manufacturing Automation include the following: Small… more
- Merck & Co. (Boston, MA)
- Job DescriptionThe Associate Vice President (AVP)/Therapeutic Area Head, Immunology Translational Medicine, will be responsible for leading the Translational ... include the clinical pharmacology support of the Common Technical Document (CTD) and label, including relevant compound/program life-cycle management.The successful… more
- Insmed Incorporated (Bridgewater, NJ)
- …in New York™, and Best Workplaces for Millennials™ lists.OverviewThe Quality Control Associate will serve as a strategic and tactical quality professional in ... ensuring timely and accurate testing, reporting, and releaseThis role will assemble, review and trend release, IPC, and stability data, generating reports as… more
- Daiichi Sankyo, Inc. (Basking Ridge, 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. (Basking Ridge, NJ)
- …study problems.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
- Insmed Incorporated (Bridgewater, NJ)
- …meetings, provides updates on health and currency of study TMF, and document tracking and currency, tracks and maintains cohesive list of protocol deviations.Reviews ... Reports and collecting TMF status updates and TMF metricsParticipates in the review of clinical trial agreements, CRO and vendor contractual documents, work orders,… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …study problems. 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
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …to post trial information on required public forums (eg.clinicaltrials.gov).Under supervision, review and document CRO-generated reports, such as site monitoring ... clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good Clinical… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …compounding ActivitiesExecute compounding responsibilities (mixer batch, tank batch, & partner batch) Document batch records with the utmost attention to detail using ... Gown properly following the standard operational proceduresRecord, maintain and review completed production documentation (batch records, log books, etc.) for… more
- Marion County (Salem, OR)
- …Marion County generated documents and documents received from other individuals/agencies. Document all targeted case management activities in a progress note per ... in case management as described in Oregon Administrative Rule ### and document per ODDS guidelines. Report Serious Events per published guidelines.Information and… more
- Kelly Services (Totowa, NJ)
- **QUALITY ASSURANCE- DOCUMENT CONTROL ASSOCIATE ** **Overview:** We are currently seeking a meticulous and detail-oriented Quality Assurance Document Control ... documents. + Develop and maintain document control procedures, including document creation, review , approval, distribution, and archival processes, in… more
- System One (Seattle, WA)
- Job Title: Quality Assurance Document Control (QADC) Associate Specialist Location: Seattle, WA Type: Contract Overview Leading Pharmaceutical company looking ... for an experienced QA Document Control Specialist. Ideal candidates should have 2+ years...technical writing skill set and be able to critically review documents while effectively inputting and expressing Quality principles… more
- CBRE (Oakton, VA)
- Associate Project Manager ( Document Control) Job ID 163353 Posted 16-Apr-2024 Service line GWS Segment Role type Full-time Areas of Interest Construction, ... - Virginia - United States of America **About the role** Overall, the Document Control Coordinator, ("DCC") shall support CBRE's client with the implementation of… more
- CBRE (Salt Lake City, UT)
- Associate Project Manager ( Document Control) Job ID 163407 Posted 16-Apr-2024 Service line GWS Segment Role type Full-time Areas of Interest Construction, ... - Utah - United States of America **About the role** + Overall, the Document Control Coordinator, ("DCC") shall support CBRE's client with the implementation of the… more
- Adare Pharma Solutions (Philadelphia, PA)
- …assistance + Performance-based bonus + Employee Recognition Programs We are seeking to hire a Document Control Associate to join our Quality Team. If any of the ... track and retrieve SOPs, protocols, reports, policies, etc. using an electronic document management system. This includes obtaining electronic review and… 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 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
