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Under the direction of the Principal Investigator(s), Co-Investigators, and Research Manager, the clinical research coordinator will be given various research duties for multiple research and quality improvement projects.
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In addition to the responsibilities above, the Clinical Research Coordinator B will assist the regulatory specialist in preparing for all local and Central Institutional Review Board (IRB) documentation through the IRB, including submissions, continuing reviews, amendments, modifications, and adverse event reporting.
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This Human Genome Editing Research Specialist C/D position requires a dynamic individual with a strong background in genome editing, laboratory management, and collaborative research efforts in the field of cell and gene therapy.
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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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Participate in clinical and technical activities pertinent to radiation oncology physics including: megavoltage photon, electron and proton therapy, CT, MR, PET/CT simulations, 3D, intensity modulated radiation therapy, and proton treatment planning, brachytherapy planning and delivery, radiopharmaceutical therapy, calibration and periodic QA of therapy equipment and patient specific QA, radiation safety procedures, special procedures (TBI, radiosurgery, etc.
$71,965.07 a yearFull-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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Understanding of CMC, QA, regulatory and clinical stages to guide preclinical activities setting up products for success at later stages. Individual will partner closely with the research team leads as well as other key stakeholders within Spark (regulatory, clinical, CMC, etc.
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Key job tasks/duties/responsibilitiesInterprets and implements quality assurance standards and procedures in accordance with the Pennsylvania Child Protective Services Law, State regulations, Philadelphia Department of Human Services (DHS) guidelines, and internal policies.
$50,000 depends on experienceFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This individual partners with Quality, Procurement, Supply Chain, Research and Development, Business unit plants, Suppliers, Brokers, and 3rd parties to actively manage Food Safety and Quality performance of Campbells supply base.
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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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The CCM Specialist 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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Demonstrates the ability to provide technical expertise and consultation to the CIO, CTO, CISO, executive leadership and other business and clinical leaders. Functions as the Subject Matter Expert (SME) to maintain an understanding of our customer’s IS business and clinical applications and the relationship to InfoSec and compliance solutions; assist Hospital stakeholders in understanding information protection needs that support the Hospital's business.
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Preferred Education:Bachelor's Degree in Engineering or a related disciplinePreferred Certifications:Biomedical Equipment Technician Certificate (BMET)Certified Biomedical Equipment Technician (CBET)Electronic Engineering Technology (EET)Additional Qualifications:Original Equipment Manufacturer or equivalent level of training on devices and systems that BME Specialist is considered expert.
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Today the FPCN serves more than 20, patients annually and is a NCQA certified Patient-Centered Medical Home and recognized by HRSA as a National Quality Leader for Behavioral Health. Assists the Call Center Manager in training call center staff on clinical updates that affect scheduling.
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On occasion, the Research Intern may be asked to perform errands which will involve walking to places within the immediate vicinity of the FIRE office. FIRE is seeking an energetic undergraduate or graduate Research Intern to aid its Research Department.
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Shift Sunday through Thursday Essential Functions and Responsibilities Perform daily GMP Quality Control laboratory testing activities at the iCTC facility with minimal to no errors while ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations Perform data analysis and final result reporting to support product lot release with adherence to turnaround times.
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clinical research quality specialist qa jobs Title: quality specialist in Philadelphia, PA
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