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Identifies and maintains key data elements, including Data Ownership, Data Lineage and the Data Glossary in Axon and EDC. Experience working with industry data governance tools, such as Axon, EDC and IDQ.
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The Explosive Detection Canine Handler partners with a trained Explosive Detection Canine (EDC) to conduct searches in/at assigned client sites, including corporate buildings, loading docks, delivery vehicles, open areas and/or other situations as needed.
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Proficiency with drug safety databases (i.e., Argus), electronic data capture (EDC) systems, Medical Dictionary for Regulatory Activities (MedDRA) and World Health Organization (WHO) Drug dictionary coding.
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MSA Security, an Allied Universal® Company, is hiring a Explosive Detection Canine Handler. Prior civilian or military K9 handler experience. Ready to make a difference as a canine handler. Our patented SmartTech® solution provides instant, remote X-ray screener support from FBI-trained bomb technicians.
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Familiarity with healthcare data domain in at least one of: electronic medical records (EHR/EMR), clinical imaging, clinical workflows; Electronic Data captures (EDC), and/or clinical research/trials.
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The College is comprised of the Folsom main campus and its two educational centers, the El Dorado Center in Placerville ( EDC ) and the Rancho Cordova Center ( RCC ). Our Strengths Folsom Lake College centers student success by providing a broad range of degree and certificate programs and student support services in different modalities (including online and hybrid) that prepare students for transfer and/or career opportunities, as well as options for student engagement, innovation, and leadership.
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Enhanced by state-of-the-art lighting, pyrotechnics and sound design, large-scale art installations, theatrical performers and next generation special effects, our events captivate the senses and inspire a unique level of fan interaction.
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PCC's clients include New York State and City agencies such as the DOT, DEP, DDC, DPR, EDC, and SCA, among others. Perfetto is seeking an experienced Bridge Construction Project Manager (Heavy Civil GC experience a must.
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Design and develop data capturing tools: Electronic Data Capture (EDC) Systems (Eg: iMedidata Rave and IBM Clinical) eCOA, IRT; Manage electronic Trial Master File (eTMF) QC review eg: Veeva Vault; Lead the Audit and Inspection/Submission Readiness activities like documentation of QC and preparing Storyboards (Eg: FDA/EMA Submissions.
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Knowledge of industry standard clinical technologies including CTMS, EDC (RAVE, InForm) Knowledge of CDISC data standards. Partner with internal and external stakeholders to ensure timely delivery of data management programming, EDC database, external data, data management programming of reports and listings including the use of visualization tools.
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Oversee vendors and actively participate in all UATs for vendor systems, including IRT, EDC, Central Labs, etc. Reporting to the Associate Director of Clinical Operations, this individual will have primary responsibility for trial management within in vivo, regenerative medicine, or oncology indications.
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Strong knowledge and experience of EDC systems (Veeva CDMS preferred); demonstrated knowledge of Microsoft Office skills and well versed in industry trends and emerging technologies supporting data collection.
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Develop and contribute to Biometrics SOPs and standard working documents meeting regulatory requirements throughout biometrics processes including IWRS/EDC, STDM, statistical programming for TLFs, and data reporting.
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Advanced understanding of cutting-edge use of Data Collection Tools (EDC systems), Data Review Tools, and/or Data Standardization methods, requirements. The SR AD, Clinical Data Engineering is a Subject Matter Expert (SME) internally in the clinical research development process through the provision of Leadership and advanced expertise in the areas of data collection/curation, data review, delivery data standardization or process definition, testing and training.
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Job DescriptionTakeda Development Center Americas, Inc. is seeking a Senior Manager, Clinical Data Management in Lexington, MA with the following requirements: Master’s degree in Pharmaceutical Sciences, Pharmacology or Toxicology or related field or foreign academic equivalent plus 6 years of related experience.
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