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The Clinical Research Coordinator (CRC) will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical studies, ensures the timely collection and management of protocol-related samples, maintains regulatory binders, and ensures study compliance with state, federal, and IRB requirements.
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Reports all incidents and breaches in the quality of care to the Clinical Pharmacy Manager, Pharmacy Operations Manager or Director of Pharmacy. Director of Pharmacy Operations Manager Clinical Pharmacy Manager Must be able to collaborate and effectively communicate with physicians, nurses and other health care professionals.
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Clinical Dietitian, Part time. Demonstrated clinical experience/competency for nutrition services in 2 or more specialty areas through at least two years’ experience in the specialty area, certification, and/or CEUs, such as sports and cardiovascular nutrition, and weight management.
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Familiarity with GCP, ICH and FDA requirements as applicable for Clinical Data Management. The successful candidate will provide clinical data management oversight of outsourced clinical trials including but not limited to project management, vendor management, coordination of internal reviews, and approval of deliverables.
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Strong knowledge of biomarker technologies and methodologies, including genomics, proteomics, imaging, and flow cytometry, as applied to clinical research. Ph. D. or equivalent degree in Molecular Biology, Biochemistry, Pharmacology, or related field with a minimum of 8 years of relevant experience in clinical biomarker research within the biopharmaceutical industry.
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We are seeking a Clinical Research Coordinator with excellent interpersonal and organizational skills. Key responsibilities will include coordination and planning with Xsphera’s vendors, hospital sites, and clients to recruit patient biospecimens, and ensure that all resources are available to efficiently execute pre-clinical drug studies using Xsphera’s ex vivo platform.
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Job Description The Clinical Educator (CE) works under the direction of Sr. Director, Education and Development to develop and deliver onboarding clinical training for new hires in Organ Donation Services (ODS), is the primary preceptor to new ODS clinical staff and assists to manage the Donation Coordinator (DC), Clinical Responder (CR) and Referral Resource Coordinator (RRC) preceptor programs.
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5 - 8 years relevant experience working as a clinical research coordinator role (project manager, research assistant, study coordinator, etc.) Experience with conduct of clinical research with pharmaceutical/device clinical trials and/or observational or social behavioral and/or public health research.
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Melrose Healthcare is seeking a Clinical Manager Licensed Practical Nurse (LPN) Nurse Supervisor. Currently seeking an exceptional Clinical Manager Licensed Practical Nurse (LPN) Nurse Supervisor to join our team in our Melrose Healthcare facility.
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The Claims Transaction Data, Data Steward is a member of a cross-functional Data Governance team who partners with business, technical, and regulatory partners to ensure the documentation and implementation of Claims Transactions data standards.
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Certification as a Certified Procurement Transplant Coordinator (“CPTC”); Certified Transplant Preservationist (“CPT”), Certified Clinical Transplant Coordinator (“CCTC”), or Certified Clinical Transplant Nurse (“CCTC.
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Creates a documentation system chronicling all incoming/outgoing clinical documentation, maintains study supply documentation, reviews Study Folder regularly to ensure file accuracy and completeness, maintains study specific metric tracking and reviews Clinical Research Associate (CRA) field monitor reports and any necessary follow-up letters in relation to specific Study Monitoring Plan, contacting CROs and CRAs, as required.
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The Senior Research Regulatory Coordinator (RC) works under the direction of the CCI Executive Director, Research Operations Director and Principal Investigator(s) to complete the regulatory requirements of clinical research projects.
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Experience providing scientific support for the development and implementation of cell therapy studies, including protocol and ICF development, electronic data capture database development, safety assessment, IB/DSUR submissions, and clinical data review.
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Comfortable working with a wide range of clinical presentations Experience with health psychology. Pay is based on several factors, including but not limited to education, work experience, licensure/certifications, scheduled clinical hours, etc.
$64,300 - $114,300 a yearExpandApply NowActive JobUpdated Today
Title: clinical Company: Cardiovascular Sys in Brookline, MA
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