- Daiichi Sankyo, Inc. (Bernards, NJ)
- …operational input into study protocol profiles, final protocols and amendmentsLead document review and coordination for the protocol and amendments. ... Directive, and International Conference on Harmonization (ICH) guidelines. The Associate Director is accountable for operational planning and execution at… 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
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …drafts meeting request based on draft BB, and effectively participates in document review .Works on additional regulatory activities per direction and strategic ... areas centered around rare diseases and immune disorders. Summary: The Associate Director, Regulatory Affairs - Regulatory Project Management (RPM) provides planning… more
- Aequor (Salt Lake City, UT)
- …and Recommendations: Participate in investigations and recommend corrective actions. 7. SOPs and Document Review : Write, revise, and review SOPs, forms, and ... be deferred to more senior QA personnel. Responsible for labeling issuance, review and/or returns; document processing including data entry, data verification… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- … Associate will support the Clinical Research team in literature searches, document generation, editorial review , and organization as well as assist with ... laboratory experiments as needed. Job Responsibilities Develop an understanding of the drug development processes within ExelaGain familiarity with product specific literature searches to gather and present information regarding the pharmacology, toxicology,… 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)
- …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. (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
- 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
- Novo Nordisk Inc. (Plainsboro, NJ)
- …planning and execution to assigned Novo Nordisk, Inc. therapeutic areas. Assist Associate Director with development and execution of annual strategic convention plan ... Relationships Reports to the Manager, Convention Marketing reports to the Associate Director, Convention Marketing of the Strategic Meeting & Event Management… 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 (St. Paul, MN)
- Job Description The Document Review Associate will be joining a team of 12 to perform Document Review according to standard procedures or ... to detail, and professionalism -Bachelors or Associates -Finance experience -Mortgage Background - Document Review Specialist Analyst or Review experience… more
- Insight Global (Jacksonville, FL)
- Job Description The Document Review Associate will be joining a team of 6 to perform clerical work such as labeling files, data uploads, Bailee processing, ... in an office setting (longevity) -Bachelors or Associates -Finance experience -Mortgage Review experience -Mortgage Background - Document Review Specialist… more
- US Bank (Jacksonville, FL)
- …and discover what you excel at-all from Day One. **Job Description** The Document Review Associate performs routine and/or repetitive clerical functions ... according to standard procedures or instructions. Responsible for researching various issues and reporting exceptions for Corporate Trust clients to ensure client satisfaction, quality control, and compliance with custodial agreements. Reviews loan (or… more
- Belcan (Stratford, CT)
- …hour Contract/Indirect Location: Stratford, CT 06615 Area Code: 203, 860 We're seeking a dedicated Document Review Associate to join our team on a contract ... Document Retention Associate Job Number: 353635...or in similar roles is a plus. Responsibilities: * Review and classify both technical and non-technical records. *… 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
