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As part of the Protein Sample Management (PSM) team, you will play a key role in managing both inbound and outbound. Contractor – Research Associate, Protein Sample Management page is loaded.
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Experience with geologic mapping, geotechnical and geophysical data collection, sample collection of laboratory analysis, experience using handheld X-Ray Fluorescence (XRF) analyzers a plus. Communicate with subcontractors, project management, and client during the implementation of field activities.
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Assist in QC sample management, including receipt of in-process samples and issuance of controlled documentation. Manage routine operations including instrument qualification and maintenance, SOP and specification documentation, raw material sampling and testing, and record-keeping.
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Cross-functional interaction, coordination, and planning/scheduling with Perfumers, Fragrance Development Managers, account teams, and sample labs. dsm-firmenich has an immediate opportunity for an organized, detail-oriented and motivated Laboratory Technician to join our Technical Development group in the Perfumery & Beauty Division located in Plainsboro, NJ. As a Laboratory Technician you will support proactive and client-initiated fragrance and technology development projects in the Air Care category.
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Working with Clinical Management Teams (CMTs) and biomarker/translational research teams to implement and execute the clinical biomarker and translational sample strategy for projects. Extensive knowledge and understanding of clinical research, ICH, GCP, GLP, data management, regulatory and legal issues/processes as they relate to biomarker samples.
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Responsible for tasks related to stability study and sample management include; intake of samples, labeling of samples, counting samples, documenting and maintaining sample inventory, staging samples for storage in stability chambers, placing stability samples in the stability chambers, pulling samples and delivery to testing labs and assisting in the processing of all related stability documentation required for shipping samples, as needed.
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Roll-out compliance communication and training actions for management and/or employees, including in the areas of customer due diligence, code of conduct, data protection, international sanctions, money laundering, anti-corruption, and fraud.
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Strong understanding and capability in change management, database analytics and development including data uploads, data identification, data formatting and data verification procedures. Minimum of 5 years’ experience working in database management in a healthcare setting.
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We are seeking a talented and motivated Civil Engineer with either an Engineer-in-Training (EIT) or Professional Engineer (PE) license, and a minimum of 3 years of experience in land development or stormwater management.
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With supervision, the Senior Scientist I will serve as study director/principal investigator to perform MD, MV/MQ and Sample analysis for Large Molecule (LM) Bioanalysis projects. Serve as a PI to independently design and perform large molecule pharmacokinetics, immunogenicity (ADA and Nab), biomarker, and enzyme kinetic analysis method development, validation and sample analysis.
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Establish quality management systems and processes to support site build activities, ensuring documentation completeness and adherence to relevant regulations. Project Management: Plan, coordinate, and oversee all aspects of cell therapy site build projects, including facility design, construction, commissioning, and validation.
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EDC design, build, UAT (CRFs and Edit Checks)Data collection, reconciliation, processing, coding, reporting, validationReview and approve data management documentation and specifications (data management plans, external data transfer agreements, validation plans etc.
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This position reports to the Launch Excellence, Project Management lead in Otsuka's Marketing Operations organization. Marketing Operations provides US launch lifecycle project management and enablement for the commercial organization, from pre-launch to Loss of Exclusivity (LoE), including brand teams and other key functional areas.
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Strategic HR business partner driving the people strategy, workforce planning, organizational design, talent management, team effectiveness and change management for Nonclinical Safety and Veterinary Sciences (NCSVS) and Cancer Immunology & Cell Therapy Thematic Research Center (CICT TRC.
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Responsible for review of study documentation for Trial Master File (TMF) quality for sponsor and/or CRO. Expert in TMF filing best practices, clinical documentation at all levels. Proficiency in Document Management (Adobe professional, knowledge of Scanning, indexing, using ISI Tools.
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sample management documentation jobs in Hopewell, NJ
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