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Licensed Clinical Social Worker — Are you ready to launch or expand your private practice?. ● You’re a fully-licensed Clinical Social Worker at a Master’s level or above with LCSW, LICSW, or LCSCW licensure (accepted on a state by state basis), a valid NPI number, and malpractice insurance.. Start taking insurance, stress-free: Get credentialed for free in multiple states in as little as 30 days and start seeing covered clients sooner.. Increase your earnings: Secure higher rates with top insurance plans through access to our nationwide insurance network.. Licensed Clinical Social Worker, mental health therapy, private practice, insurance credentialing, medicare, medicaid, practice management, patient care, behavioral health, clinical counseling
The ideal candidate will have a strong background in healthcare administration, regulatory compliance (Medicare Conditions of Participation), clinical coordination, and business operations.. Manage all aspects of the agency’s clinical and administrative operations, including staff supervision, patient care coordination, budgeting, and resource allocation.. Maintain continual survey readiness and lead the agency through state, CMS, and accrediting body inspections (e.g., Joint Commission, CHAP, ACHC).. Ensure appropriate supervision and support of clinical staff including RNs, PTs, OTs, SLPs, MSWs, HHAs, and administrative personnel.. Comprehensive knowledge of Medicare regulations, OASIS documentation, HIPAA, and CMS guidelines.
Genie Healthcare is seeking a travel nurse RN Research / Clinical Research for a travel nursing job in Washington, District of Columbia. Pay package is based on 12 hour shifts and 36.0 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Genie provides travel RN’s flexibility, support, top pay scale, housing and the 1 rated, multi-state health insurance coverage. Growing from a small team of eager recruiters to a company with satisfied clients in nearly every corner of the nation, delivering excellence in patient and customer care is the key to Genie’s success. The management team has 20 years of experience in workforce solutions and staffing in medical and non-medical fields, roles ranging from Clerical job to Cardiologist to software developer to CEO.
Overview: At Genesis Healthcare, we are dedicated to improving the lives we touch through the delivery of high-quality care and exceptional service. Responsibilities: The MDS Coordinator is responsible for the coordination and completion of clinical assessments, supporting documentation, care planning and transmitting the MDS, as required by federal and state regulations. Communicate with the Business Office Manager regarding case-mix data required for billing. Educate the interdisciplinary team on case-mix and the nursing staff in terminology, language, and format that is required by MDS Qualifications: *Must be a graduate of an accredited School of Nursing with current LPN licensure in the state of employment. Experience with Medicare/Medicaid reimbursement, MDS completion, clinical resource utilization and/or case management is highly desirable.
As a Registered Nurse, you will play a vital role in promoting and restoring patients' health by completing the nursing process.. This involves collaborating with physicians and multidisciplinary team members to provide physical and psychological support to patients, friends, and families.. This is an exciting opportunity to join a dynamic team of healthcare professionals who are dedicated to delivering exceptional patient care.. Complete the nursing process to promote and restore patients' health. This position is located in a long-term care facility where you will have the opportunity to work with a diverse range of patients and colleagues.
Suburban Hospital is a member of Johns Hopkins Medicine and has served Montgomery County and the surrounding area for more than 65 years.. The designated trauma center for Montgomery County, Suburban Hospital is fully accredited by the Joint Commission and has earned ANCC Magnet Recognition for nursing excellence.. At Suburban Hospital, our greatest passion is our staff members' commitment to delivering the best patient- and family-centered care possible.. The Patient Care Tech (CNA) on our 24-bed Ortho/Neuro Unit is a critical part of the Patient Care Team and works in a collaborative relationship with the Registered Nurse (RN) and other members of the multidisciplinary healthcare team.. American Heart Association CPR/BLS certification is required.
Provides wound care to promote healing and maintain structural integrity of the skin.. Performs skin care and hygiene and reports impaired skin integrity and/or wound impairment.. Provides orthopedic/rehab device care: e.g. braces, splints, CPM. Dons/doffs compression wraps/stockings.. Current Maryland state certification as a Certified Nursing Assistant (CNA) or Geriatric Nursing Assistant (GNA) required.. Demonstrates the ability to perform delegated nursing tasks according to the age, culture, ethnicity, spirituality, and individual diagnostic needs of the persons served.
Explore how you can follow your passions and shed light on meaningful ways to serve, grow, and shine together. Assists in counseling guest/resident, family or responsible party during difficult transitional care periods. Attends regular meetings; Stand Up, Cross Over, Department Head Meetings, Town Hall, Quality Assurance and Performance Improvement (QAPI), and others as directed by the Executive Director. A minimum of two (2) years' experience in a nurse management position within a skilled nursing environment including hiring staff, coaching, performance management daily operations supervision, discipline and counseling.. Proficiency in Medicare, Minimum Data Set (MDS) / Resident Assessment Instrument (RAI), Care Plan process
Join Our Team at Mercy Medical Center Now Hiring a Nursing Support Technician.. Successful completion of CNA/GNA course and/or successful completion of Fundamentals and one additional clinical course in an accredited nursing program.. Discounts on auto & home insurance and Verizon plans. Mercy Health Services is sponsored by the Sisters of Mercy.. We are an Equal Opportunity Employer (EEO) recruiting talent for Mercy Health Services, which serves the greater Baltimore Metro and surrounding Maryland areas.
This Quality Assurance role for the JPM CBRN Task Order 3 contract in the RAQA Program Office shall perform at a subject matter expert level by providing advice and aid in the implementation of quality systems and procedures to ensure compliance with all applicable laws, regulations, and organizational quality standards in support of advanced development activities.. Lead the development and review of regulatory document for submission to FDA or other National Regulatory Authorities (NRAs) and coordinates/prepares and maintains FDA filings (such as INDs, NDA, BLAs, PMA, 510(k), EUA, etc.). Collaborate and network with internal/external regulatory professionals and clinicians, as well as investigators and researchers, and other scientific and technical disciplines to maintain current knowledge in the Chemical, Biological, Radiological, and Nuclear (CBRN), Emerging Infectious Disease (EID), and other relevant emerging and re-emerging threat spaces.. Technical Competency: GMP, GDP, GCP, GLP, ICH, Quality Audits, Quality Reviews, Experience with computerized systems and GxP compliance requirements, involving both on-premises and hosted environments.. Experience with medical product development requirements under the FDA Animal Rule regulatory pathway, including animal model development, pharmacokinetics, pharmacodynamics, and toxicity desired.
Proficiency in Electronic Health Records (EHR) systems. We are seeking a Per Diem Employee Health Nurse (RN) to join our healthcare team in Baltimore.. Implement infection prevention protocols and conduct exposure investigations. Participate in employee wellness initiatives and health promotion activities. Come join UMMC and discover the atmosphere where talents and ideas come together to enhance patient care and advance the science of nursing.
The Frederick National Laboratory is 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.. The Vaccine, Immunity and Cancer Directorate (VICD) at the Frederick National Laboratory investigates immune responses to vaccines in preclinical and clinical studies.. To address gaps and unmet needs in serology assay development and standardization and to gain a solid fundamental knowledge of the immune response to underlying mechanisms of protection against infection, leveraging the vast expertise and excellence in HPV serology at the FNL. Experience in quality control and quality assurance related to immunology, virology and/or molecular biology procedures for reagent production and assay development and performance.. Experience working with standards and reference materials, immune assay (ELISA, multiplex assays) development and validation.
The University of Maryland School of Medicine has exciting opportunity for Clinical Research Nurse to join the Division of Addictions Research and Treatment in the Department of Psychiatry.. The Clinical Research Nurse will assist in the administration of NIH-funded, multi-site clinical trials investigating interventions with patients engaged in outpatient and office-based addiction treatment programs.. The Clinical Research Nurse will work in collaboration with lead and local site investigators to implement protocols and carry out day to day study activities at University of Maryland addiction programs.. The Clinical Research Nurse will support division faculty initiatives and studies as assigned.. Other: May require training related to occupational safety and health, environmental compliance, shipping of hazardous materials and/or ionizing radiation May substitute additional years of relevant experience in lieu of minimum education.
As a Field Medical Director, MSK Surgery you will be a key member of the utilization management team.. Utilizes medical/clinical review guidelines and parameters to assure consistency in the MD review process to reflect appropriate utilization and compliance with SBU`s policies/procedures, as well as Utilization Review Accreditation Commission (URAC) and National Committee for Quality Assurance (NCQA) guidelines.. May assist the Senior Medical Director in research activities/questions related to the Utilization Management process, interpretation, guidelines and/or system support.. Participates in on-going training per inter-rater reliability process.. Not under current exclusion or sanction by any state or federal health care program, including Medicare or Medicaid, and is not identified as an "excluded person" by the Office of Inspector General of the Department of Health and Human Services or the General Service Administration (GSA), or reprimanded or sanctioned by Medicare.
Medical Director - Endocrinology (Obesity). A growing biotech with an expanding late-phase pipeline is seeking an experienced Medical Director to lead clinical development efforts in endocrinology, with a focus on obesity.. Contribute to and execute the Clinical Development Plan for obesity programs. Partner with cross-functional teams including Clinical Operations, Regulatory Affairs, Biostatistics, and Medical Affairs. MD (Board Certification or PhD in Endocrinology or related field preferred)
Certified Nursing Assistant/Caregiver (CNA/GNA). Leaders in our industry, Interim HealthCare is hiring Home Health CNAs who are committed to providing exceptional patient care and eager to grow in their career.. Help with daily activities (ADLs) such as bathing, toileting, dressing, grooming, hygiene, nail/skin care, eating and nutritional intake. Active Certified Nursing Assistant (CNA) license. Join a nationwide network of CNAs who are making a significant difference in the lives of others through the personalized, home-based care they provide.
In addition, the Director Quality Assurance provides strategic planning for continuous improvement and reporting/escalation of quality issues and/or risk mitigation activities.. Facilitate the Quality Management System, including the Quality Manual, and provide an on-going assessment of QMS effectiveness via monthly Quality Management Review meetings with cross-collaboration from each function.. Facilitate the internal audit program, including oversight of audit schedules, plans, and follow-up according to internal procedures, regulatory guidance / expectations, and auditing best practices in alignment with compliance policies and standards.. Act as the negotiator with regulatory agencies on quality related matters, involving and coordinating with the business to maintain, resolve or improve company’s compliance standing.. Bora Pharmaceuticals is focused on developing and manufacturing branded, generic and over the counter (OTC) healthcare and pharmaceutical products for patients around the globe.
LMI is seeking an experienced Regulatory Affairs Manager to support the Office of Human and Animal Research Oversight (OHARO), Office of Human Research Oversight (OHRO) at Ft. Detrick in Frederick, MD location.. Will serve as lead auditor for quality audits (GMP & GLP) of developing and manufacturing investigational countermeasures for MCS. This position can be performed hybrid/remotely with onsite requirements 1 day per week.. Founded in 1961 to help the Department of Defense resolve complex logistics management challenges, LMI continues to enable growth and transformation, enhance operational readiness and resiliency, and ensure mission success for federal civilian and defense agencies.. GCP compliance audits of investigator sites, CRO facilities, and vendors, including clinical sample labs in accordance with audit plans. Experience serving as a Regulatory Affairs Manager performing:Laboratory and facility inspections in support of GLP studies Facility audits as required by GLPs QMS audits of ISO/FDA elements Regulatory agency inspectionsGCP training GCP compliance audits Internal and external current GMP audits
Regulatory Affairs Manager. LMI is seeking an experienced Regulatory Affairs Manager to support the Office of Human and Animal Research Oversight (OHARO), Office of Human Research Oversight (OHRO) at Ft. Detrick in Frederick, MD location.. Will serve as lead auditor for quality audits (GMP & GLP) of developing and manufacturing investigational countermeasures for MCS. This position can be performed hybrid/remotely with onsite requirements 1 day per week.. Founded in 1961 to help the Department of Defense resolve complex logistics management challenges, LMI continues to enable growth and transformation, enhance operational readiness and resiliency, and ensure mission success for federal civilian and defense agencies.. Experience serving as a Regulatory Affairs Manager performing:Laboratory and facility inspections in support of GLP studiesFacility audits as required by GLPsQMS audits of ISO/FDA elementsRegulatory agency inspectionsGCP trainingGCP compliance auditsInternal and external current GMP audits
The Regulatory Affairs Manager V (Regulatory Affairs) for the JPM CBRN Task Order 3 contract shall serve as a liaison at the One RAQA Program Office, between the AJPEO MRAS regulatory office and product leads to ensure DoD-funded regulatory Sponsors developing MCMs are complying with relevant laws, regulations, and current guidance's. Provide input to Sponsors' regulatory documents for submission to FDA or other National Regulatory Authorities (NRAs) and coordinates/prepares and maintains FDA filings (such as INDs, NDA, BLAs, PMA, 510(k), EUA, etc. Collaborate and network with internal/external regulatory professionals and clinicians, as well as investigators and researchers, and other scientific and technical disciplines to maintain current knowledge in the Chemical, Biological, Radiological, and Nuclear (CBRN), Emerging Infectious Disease (EID), and other relevant emerging and re-emerging threat spaces. Bachelor's or Master's degree in Life Sciences, Public Health, Medical, Nursing, Pharmacy, Veterinary, Epidemiology or a related discipline, as well as fifteen (15) years of general experience and ten (10) years of relevant experience. Experience with medical product development requirements under the FDA Animal Rule regulatory pathway, including animal model development, pharmacokinetics, pharmacodynamics, and toxicity.