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The Clinical Research Coordinator A will also be responsible for training new personnel who will be working on clinical trials within the division. The Clinical Research Coordinator A will recruit and screen patients as outlined in research protocols, will coordinate all research visit activities for assigned projects (including processing and shipping blood and urine samples), and will assist in the maintenance of research records in compliance with IRB and HIPAA regulations.
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This includes, but is not limited to, activities to advance health equity and disparities-focused study designs, community-academic partnerships and stakeholder engagement, inclusion and representativeness in CHOP clinical trials, interpretation and dissemination of findings in non-academic settings, and equitable translation (e.g., health services and policy research) of novel discoveries to advance patient care.
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Clinical Research Nurse C ResponsibilitiesWork in collaboration with Research Team Leaders and Principal Investigators with initiating study procedures for new IITs and industry-sponsored clinical trials.
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The Division s clinical trial portfolio is further enhanced by an outstanding Phase I program, in academic partnership with the Sarah Cannon Research Institute (SCRI), and a strong and innovative Health Delivery Research group.
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Clinical Research Coordinator A (Department of Pulmonary,Allergy and Critical Care) The Clinical Research Coordinator A will perform a range of activities in the management of several cohorts of patients with critical illness including sepsis, pneumonia and acute respiratory distress syndrome (ARDS.
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Familiarity with gene therapy or rare disease therapeutics development process including patient selection for clinical trials. Demonstrated working knowledge of design controls, analytical, clinical, and manufacturing process validation requirements for IVDs, GCP, GLP, and GMP requirements; working knowledge of requirements for US and global regulatory submissions related to IVDs for use in clinical trials and for commercialization of companion diagnostics.
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Working Conditions:Anticipated travel of up to 30% to locations which may include the following: World Headquarters (WHQ) Office, Research Kitchen, Pilot Plant, and Manufacturing Plants (Campbell Soup Company (CSC), co-manufacturers and vendors.
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Under the direction and guidance of the principal investigator (PI), they will provide analytic support for research involving prospective data from clinical trials and observational studies, electronic health records, large administrative, claims, and echo imaging databases.
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Prior research experience in a healthcare setting*Prior research experience with NIH-sponsored research studies, industry clinical trials, and investigator-initiated research studies.
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The Associate Principal Scientist will work closely with individuals from PaCES, Clinical Research, Regulatory Affairs, Biostatistics, Outcomes Research, and Operations to ensure COA endpoint strategies are consistent with and correctly executed to support the product strategy.
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SUMMARY JOB DESCRIPTIONThe Clinical Informatics Specialist’s primary roles are to provide project management, software support and training for the PHMC Health Network’s clinical systems, electronic medical record (EMR), and other applications.
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Essential Functions Lead Innovation Team in the research and development of project-related microelectronics including strategy, design, analysis, modeling, development, prototyping, testing, circuit design, ASIC design, systems integration, and production.
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Support Staff: Our team includes a dedicated MA/X-ray Tech/Clinical Office Manager to assist you in providing excellent patient care. As a member of our team, you will work alongside another provider during each shift, supported by our dedicated MA/X-ray Tech/Clinical Office Manager.
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8 years experience in medical coding (physician), billing and coding auditing, compliance, clinical documentation and coding training (Required) Temple Health refers to the health, education and research activities carried out by the affiliatesof Temple University Health System (TUHS) and by the Lewis Katz School of Medicine atTemple University.
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Required Licensure: Licensed Social Worker (LSW), Licensed Professional Counselor (LPC), Licensed Marriage and Family Therapist (LMFT), Licensed Clinical Social Worker (LCSW) The Clinical Care Manager must utilize clinical knowledge of best practices and evidence-based treatments to ensure CBH members receive timely access to quality, medically necessary behavioral health services.
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clinical trials research jobs Title: clinical research nurse Company: Highmark Health in Philadelphia, PA
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