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Responsible for the preparation of relevant content for global clinical documents (CTPs, IBs, CTRs, ICFs, or other relevant clinical documents) including the planning and set up in the document management system for authoring teams, the planning and strategy for document development, and the overseeing of timelines.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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With your knowledge in GMP you contribute to daily operations to support project work, trial management and supply chain activities for Clinical trials supplied by CTSU. Thanks to your expertise in clinical supply chain management, you are responsible for generating and providing reports from several systems to support global CTSU management and medical budgeting.
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Thanks to your expertise in clinical supply chain management, you are responsible to generate and provide reports from several systems to support global CTSU management and medical budgeting.
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Utilizing knowledge in GMP, contribute to daily operations to support project work, trial management and supply chain activities for Clinical trials supplied by CTSU. What You Need to Bring to the Table: Bachelors' Degree 3-5 years working in Pharmaceutical Industry GMP and GCP Pharmaceutical Industry Regulations knowledge.
$45 - $55ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Our popular service niches that earned us global accolades are: clinical data management, clinical analytics, patient-centric technology enablement services, statistical analysis and reporting services, data anonymization services, RWD aggregation and curation services etc.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The success of global medical affairs (GMA), MA, and our asset programs is highly dependent on this role through strategic leadership and partnership with TAs, corporate functions (Healthcare Affairs/Patient Engagement, GoToMarket (GTM) governance and capability leaders), technology partners, regions, and countries.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Experience in supply chain management, contribute to maintain and improve the global CTSU project plan templates in Planisware and act as CTSU Key-user role to ensure correct CTSU detailed project plans for all NBE, NCE and NTM trials include sponsored trials for commercial products.
$45.52 - $53.52 an hourExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Partner with a mentor who is a seasoned professional engineering manager to develop best practices and evolve into a leader at SchaefflerGain knowledge alongside experts in areas such as quality, project management, and program management.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Utilizing knowledge in GMP, contribute to daily operations to support project work, trial management and supply chain activities for Clinical trials supplied by CTSU. Utilizing experience in supply chain management, contribute to maintain and improve the global CTSU project plan templates in Planisware and act as CTSU Key-user role to ensure correct CTSU detailed project plans trials for commercial products.
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Work with Reinsurance Finance staff and Collections management team to conduct research into reinsurance recoverables and contribute towards completion of periodic reporting. In-depth knowledge of loss allocations across multiple underwriting years and the application of claims to reinsurance that includes AP&H claims.
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You will serve as a key contributor to daily department operations; supporting third party service provider selection, negotiations and contract development, budget preparation, cost management, allocation and invoicing, operational enhancements and strategic projects in the insurance field and cross training of department colleagues to enhance teamwork and knowledge.
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With your experience in supply chain management, you contribute to maintain and improve the global CTSU project plan templates in Planisware and act as CTSU Key-user role to ensure correct CTSU detailed project plans for all NBE, NCE and NTM trials incl.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Your Key ResponsibilitiesSchaeffler, a global automotive and industrial supplier, is seeking eager Engineers for our manufacturing facility in Danbury, CT. This is a two-year development program comprised of four six-month rotations that provide cross-departmental exposure for the Quality career path.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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GMP and GCP Pharmaceutical Industry Regulations knowledge. In your new role as Project Office Specialist, you closely collaborate with the Head of the Project Office to set-up and continuously develop the new Global CTSU Project Office.
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Job Title: Project Office Specialist. Location: Ridgefield, CT (Hybrid) MS Teams Meeting or Virtual Meeting software experience. IIS and BI sponsored trials for commercial products. SAP software based computer systems experience.
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knowledge management global jobs in Ridgefield, CT
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