Clinical Trials Project Coordinator — Data & Documentation
Canfieldpublishing
Canfield Scientific, Inc. is seeking a Clinical Project Associate to join our Clinical Services team in Parsippany, NJ. This role supports designated clinical project teams with project management, documentation, and data activities in a fast-paced environment. The ideal candidate has an associate degree or 1 year of experience, strong Microsoft Office skills, and excellent time management, communication, and team collaboration abilities. Competitive hourly pay and comprehensive benefits offered. #J-18808-Ljbffr Canfieldpublishing
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...and Europe, the firm provides support on projects of varying size and complexity. Together,... ...to take ownership of project controls and document management on one of the most high-... ...Proficient in workflow design, form creation, and data/report configuration within e-Builder....DataFor contractorsLocal area- ...is seeking an Environmental Assistant Project Manager for our client's team. Our... ...combination of project management, technical documentation, field coordination, environmental compliance, and client... ...Review project documentation, field data, laboratory analytical results, and...DataFull timeFor contractorsFor subcontractorWork at officeLocal area
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Join a Team That’s Advancing Clinical ResearchWe’re looking for a passionate... ...high-quality clinical trials. In this role, you’ll partner... ...protocol compliance, data integrity, and high-quality study... ...data qualityMaintain accurate documentation and contribute to inspection...DataFull timePart timeImmediate startWorldwide- Canfield Scientific, Inc. is seeking a Clinical Project Associate who can prioritize, multitask, and communicate clearly in a fast... ..., timelines, and project specifications, and involves document handling and data management. Ideal candidates have an associate degree or...DataWork at office
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...ies) and reporting study data as required by the study... ...contracted scope of work and Good Clinical Practice.• Work with... ...plan in line with project needs to enhance predictability... ...(as required) site documents are available for filing in the Trial Master File (TMF) and verify...DataFull timePart timeLocal areaImmediate startWorldwide$75k - $95k
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...Biometrics you will be part of clinical development teams,... ...support both traditional clinical trial activities and broader evidence... ...integrating clinical and real-world data to inform development and... ...plans and submission documentation to inform business and scientific...DataFull timeTemporary workLocal areaFlexible hours- ...you, then apply below. Project Manager – Next Best Engagement... ...marketing and commercial data into actionable insights for... ...Technology and Architecture Coordination Serve as the bridge between... ..., including required documentation, stakeholder sign-offs, and...DataWork at office
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