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Experience and/or knowledge of the 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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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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Strong hands-on SAS programming skills, expertise in EDC databases, CDASH, CDISC, and SDTM/ADaM standards, medical coding dictionaries, controlled terminologies, as well as in industry standards for electronic submission of data to FDA.
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Previous experience with EDC systems (eClinical, Medidata RAVE, InForm), and electronic Trial Master File systems. Previous experience with EDC systems (eClinical, Medidata RAVE, InForm), and electronic Trial Master File systems.
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Familiarity with common software and technologies used in clinical data science (e.g., SAS, R, Python, Rave, Veeva). Integrate expertise in EDC, RWE and external data to optimize data collection and standardization.
$224,000 - $233,000 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Founded in 2015, the company has built a portfolio of 20+ drug development programs ranging from preclinical to late-stage development in multiple therapeutic areas including genetic dermatology, precision oncology, cardiology, endocrinology, neurology, pulmonology, and renal disease, with two approved drugs.
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Experience configuring Rave EDC to CTMS is a big plus. An ideal candidate would be experienced with python and can own the management of custom EDC to CTMS solution - Including CI/CD in Azure DevOps, understanding of SDLC principles in regulated industry.
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Custom reporting using Business Objects, SAS, Python, Crystal Reports, and understanding of Medidata Rave Study Build is required. Custom reporting using Business Objects, SAS, Python, Crystal Reports, and understanding of Medidata Rave Study Build is required.
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Experience with clinical trial databases (e.g., Medidata Rave, InForm, etc. Experience with clinical trial databases (e.g., Medidata Rave, InForm, etc. Knowledge of FDA regulatory requirements and ICH/GCP guidelines.
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Experience with web-based EDC (IBM Clinical preferred), clinical data management systems and medical coding dictionaries such as MedDRA and WHO Drug. background in programming is preferred. Responsibilities: Develop requirements for EDC including CRF and system design; performs and organizes all aspects of the clinical database build and cross-functional User Acceptance Testing (UAT.
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Experience with web-based Electronic Data Capture (EDC), clinical data management systems and industry wide thesauri, such as MedDRA and WHO Drug. Provides training on the CRF completion guidelines and EDC system at Investigator meetings and to internal or external team members, as needed.
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G., Medidata Rave, InForm, etc.) G., Medidata Rave, InForm, etc.) Experience in all aspects of protocol conduct, both early and late phases, including protocol writing, start-up, study execution, analysis, and reporting Sufficient content expertise to be able to meaningfully contribute to document development and data review and interpretation under the direction and oversight of the CMO. Knowledge of applicable FDA Code of Federal Regulations, Good Clinical Practices, and clinical trials guidelines is required.
$250,000 - $315,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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We hear our customers frequently rave about our product, for example "we've seen north of 10x ROI on our annual investment in Haus in the first 2 months alone.” Our ideal candidate has experience in product marketing, product management, or sales enablement in a high-growth B2B SaaS environment, and brings together strong strategic instincts, curiosity, structured communication skills, creativity, and a bias towards action.
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In fact, our flexible-hybrid approach to work is one of the things our employees rave about. Ability to be a user experience design leader, including usability principles, user research methodology, testing techniques (A/B, Multi-Variant), design theory, and interaction design.
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Responsible for all new patient triage for Outpatient Psychiatry Clinic, EDC Admission and Consultation Services. The Peds Psych Intake Coordinator Lead is responsible for coordinating all aspects of the patient intake process by overseeing insurance verification, pre- certifications, authorizations, referrals, intake screenings and patient scheduling.
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rave edc jobs in Palo Alto, CA
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