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The C-WMD Systems Group develops innovative systems and technology for prevention, preparedness, characterization, detection, mitigation, medical response, remediation, and attribution of CBRNE (Chemical, Biological, Radiological, Nuclear, and Explosive) and related threats.
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The approach the team takes will incorporate clinical trial data, real world evidence data, clinical free text, medical imaging, patient reported outcomes, and device data to define new digital approaches to addressing the pressing problems across the AZ R&D portfolio.
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Ocean Winds (OW Offshore, S.L.), a 50/50 joint venture by EDP Renewables (EDPR) and ENGIE, has brought its experience, skills and knowledge to the United States, one of its target areas for future growth.
$130,000 - $150,000 a yearFull-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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Health Savings AccountCCRM Paid Family Medical Leave (eligible after 1 year)Supplemental Options (Critical Illness, Hospital Indemnity, Accident)Professional Development, Job Training, and Cross Training Opportunities Bonus PotentialWhat You Will Do:The Clinical Laboratory Technician is responsible for andrology and endocrinology procedures, maintenance of computer-generated logs and reports related to patient testing and billing, and other lab related duties.
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The Department of Chemical Engineering seeks applications for open-rank (Assistant, Associate, or Full Professor), interdisciplinary faculty candidates with research interests focused within the food, water, energy nexus.
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We have an immediate opening for a full-time, medical/scientific Writer & Content Developer for Medical/Pharmaceutical/Biotech education. Education + ExperienceMS or PharmD degree in life science, healthcare, communications, journalism, or medical/science writing; and/or 2 years of medical/scientificwriting experience creating educational,instructional, or training materials.
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Press and Videos: [CEO Blog Post] [Tech Crunch][Forbes] [Fortune] [Forward]You WillWork alongside physicians to provide personalized primary careUse clinical skills for lab collection, testing, medical proceduresAssist in care coordination of the patient experienceAssist in building medical policies and proceduresPerform back-of-house clinical diagnosticsCollaborate with multidisciplinary team of engineers, designers, physicians, and nursesYou AreImpact-driven.
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Knowledge of and experience with medical terminology, controlled terminology, clinical data standards is a plus. The Clinical Data Analyst partners cross functionally to identify risk to data integrity throughout the data flow to drive quality collection for non-EDC data sources (fluid & tissue labs, digital, imaging, wearables) in Dyne's clinical studies.
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Position Summary Working closely with the Associate Director, Clinical Operations, the Clinical Trial Associate/ Sr. Clinical Trial Associate (CTA) position will assist with daily clinical trial execution activities including enrollment management, vendor oversight, and the coordination of documents associated with the conduct of investigational clinical studies in accordance with applicable regulations, Good Clinical Practice (GCP), and CRISPR Therapeutics standard operating procedures (SOPs.
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Actively identify opportunities to improve clinical workflows and implement recommendations Practice Assistant: duties which include but not limited to check in and out, insurance verification, triage phone calls, scanning, and all other administrative duties assigned.
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Required Qualifications: Â Able to obtain Board Certification as a Physician Assistant, Certfied Pediatric Nurse Practitioner (CPNP) or Family Nurse Practitioner (FNP) Able to obtain Unlimited Licensure in the state of Massachusetts A minimum of 3 years of experience working in pediatric urgent care or emergency medicine Active DEA License.
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Responsible for managing the clinical trial data queries along with the planning and execution of medical coding and SAE reconciliation. Deep understanding of drug development, study conduct processes, GCP and regulations related clinical data management as well as ICH guidelines, FDA/EU regulations.
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Quipt Home Medical is a rapidly growing leader in the provision of clinical respiratory equipment and service in the durable medical equipment industry. The Respiratory Sales Specialist provides clinical and educational tools and programs to ensure successful understanding and application of the respiratory product line.
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A minimum 5+ years of experience in Clinical Operations roles within the Pharmaceutical and/or Medical Device Industry, with heavy concentration within clinical trial management and monitoring.
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Partners with Clinical Operations, Medical Affairs/local country offices to obtain local insights into country and site selection. The Clinical Trial Manager, Site Start-up will lead internal process improvements related to study start up activities to ensure clinical trials are executed with high quality standards in compliance with regulatory requirements, GCP, and company SOPs. This role is based in our Waltham, MA headquarters.
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Title: medical assistant clinical Company: Piedmont Urgent Care By Wellstreet in Waltham, MA
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