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Master's Degree, clinical experience, and current / active licensure in Maryland as LCPC, LGPC, LCSW-C, or LMSW. We credential you, manage paneling, insurance authorizations, and intake as our goal is to have your focus on providing excellent clinical care.
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The Clinical Manager at Kolmac Integrated Behavioral Health and all of its subsidiaries ("Kolmac" or the "Company") is ultimately responsible for the daily administration and supervision of Kolmac-CCG delivery of clinical services.
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Is skilled in Motivational Interviewing, Cognitive Behavioral Therapy, Trauma Informed Care and Trauma Informed Treatment Approaches, andassists in training clinical staff in these approaches. The Clinical Manager has responsibility for the long and short-term planning, program evaluation, and compliance with federal, state, local, and independent regulatory statutes.
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LAB Division: MLT, LT, Clinical Lab Scientist, Histology Tech, Cyto Tech, Phlebotomist. Imaging Division: Rad Tech, CT Tech, MRI Tech, Ultra Sound Tech, Nuc Med Tech, US Gen/Vasc, LAB Division: MLT, LT, Clinical Lab Scientist, Histology Tech, Cyto Tech, Phlebotomist.
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The Mental Health Professional Counselor Advanced is the advanced level of professional counseling work, at the Licensed Clinical Professional Counselor level, providing counseling services as an expert to youth involved with the Department of Juvenile Services.
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Minimum 3-5 years clinical experience in any of these areas: acute care, home health, physician office management, managed care organization, provider relations, pharmaceutical sales. Actively participate in team huddles and contribute to clinical learning.
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Direct experience with the following tasks: Clinical intake, patient data collectionLaboratory specimen collection (blood-draw/venipuncture, urine collection, point of care testing, etc.) Our Medical Assistants also: Perform Clinical Intake with patients to include taking and recording vital signs and patient historyAssist patients as needed with walking, transfer, specimen collection, exam preparation, etc.
$3,500Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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The Frederick National Laboratory is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI) and operated by Leidos Biomedical Research, Inc. The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases.
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Maintain the Trial Master File, along with the QA Manager and Clinical Project Manager. POSITION SUMMARY:We are seeking a capable Jr. Clinical Research Associate (CRA) to be responsible for assisting the clinical team in planning, initiating, and monitoring Clinical trial sites as well as tracking enrollment and site engagement activities.
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Comply with electronic medical records (EMR); complete clinical notes/documentation; uphold 48-hour documentation standard. Completes clinical notes and other paper work as required within documentation deadlines.
$60,000 - $120,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Responsibilities are focused on the management and career development of the organization's Clinical Research Associate (CRA) workforce as well as supporting the development of departmental initiatives to strengthen the quality and productivity of GCM operations.
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Assist Clinical Scientist, Study Responsible Scientist (SRS), &/or Study Responsible Physician (SRP) in various clinical research assigned Immunology Development clinical trials. Assist with clinical study activities such as study start up, investigator meetings, data review, etc.
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A Master's level education degree from an accredited School in Speech Language Pathology, Certificate of Clinical Competency (CCC) or a Clinical Fellow (CF) in process of obtaining a Certificate of Clinical Competency through the American Speech Language and Hearing Association (ASHA) Board.
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Vector Biomed aims to become a leading supplier of high quality Lentiviral vectors for research and clinical use. Team members will support both pre-clinical and GMP Quality Control release testing in a dynamic new company setting.
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You will drive all aspects of the downstream marketing for NGS product lines focused on clinical hematology-oncology. Guide the development of copy and creative content for NGS clinical hematology-oncology markets, appropriately positioning products within compliance guidelines, while conveying strong value propositions and clear product differentiation.
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clinical job Company: Johns Hopkins University in Frederick, MD
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