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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 - RN is responsible for the timely and accurate completion of the MDS treatment assessment tool and for reviewing care plans and their delivery for factors specific to our patients/residents such as physical, cognitive, and socialization factors to ensure compliance with our high standards of care.. Conduct concurrent MDS reviews to assure achievement of maximum allowable RUG categories.. Integrate information from nursing, dietary, social services, restorative, rehabilitation, and physician services to ensure appropriate reimbursement.. LPNs with MDS experience may be considered.
The Traveling Orthodontics Treatment Coordinator serves as a key member in the patient experience and flow. High School Diploma or GED with 4 or more years experience in a dental office environment.. Ideal candidates will have a Bachelor s degree in Healthcare Administration, Medical Sales or other related degree.. Strong computer skills including: Microsoft Office and Healthcare Practice Management systems.. Superior patient experience skills and successful track record of positive patient communications
Overview Join our team as a evening shift, full-time, Recovery Room (PACU) Registered Nurse (RN) in Tulsa, OK. Why Join Us?. Thrive in a People-First Environment and Make Healthcare Better Thrive: We empower our team with career growth opportunities, tuition assistance , and resources that support your wellness, education, and financial well-being.. People-First: We prioritize your well-being with paid time off, comprehensive health benefits, and a supportive, inclusive culture where you are valued and cared for.. Qualifications Job Requirements: Graduate from an accredited school of nursing Current Registered Nurse license in Oklahoma BLS Certified ACLS and PALS must obtain within 6 months of hire.. Preferred Job Requirements: One year experience as a Registered Nurse in a peri-anesthesia or critical care environment.
If you’re passionate about making a difference and thrive in a collaborative setting, New Bridge Medical Center is looking for a Certified Nursing Assistant.. Takes and records TPR, blood pressure and reports deviations from normal to Primary or Charge Nurse.. Assists patient with activities of daily living including skin care (e.g., bathes, dress, helps patient ambulate).. Communicates effectively with Charge Nurse/Primary Nurse regarding patients’ needs and requests.. Maintains established departmental policies and procedures, objectives, quality assurance program, safety, environmental, and infection control standards.
Join Diversicare's Dynamic Team as a CNA/STNA!. As a Certified Nursing Assistant (CNA) or State Tested Nursing Assistant (STNA), your outstanding patient care skills are highly sought after.. Career Growth: Unlock opportunities for advancement through cross-training and shadowing in diverse departments like Medication Tech, Workforce Manager, Activities and beyond!. Competitive Compensation: Enjoy top-tier wages, with daily wage access and a comprehensive benefits package including medical/dental/vision, 401(k), vacation, and tuition reimbursement.. Cultivate meaningful relationships with patients, families, and colleagues, fostering a warm and caring environment.
Occupational Therapy (OT). Rehab Therapy - Occupational Therapy (OT). Complimentary Onboarding: We cover the costs of your onboarding process, including physicals and TITERS. With a dedicated Onboard Specialist, you can focus on patient care while we handle the details, helping you get started faster.. 24/7 On-Call Support: Our experienced team is available around the clock, providing clinical support whenever you need it.. Quality Assurance: With the Joint Commission's Gold Seal of Approval for Health Care Staffing Services Certification, you can trust that you're part of a reputable organization committed to excellence.
We are seeking a Group Vice President, Legal Affairs to serve as a broad-based utility player and trusted business partner to our General Counsel and executive team. This is a generalist role designed to provide coverage across core in-house legal needs, allowing company to thrive, legal department to excel, and the business to move with confidence. Insurance: Oversee corporate insurance programs and claims management. Proven ability to support and amplify the GC while operating independently when needed. Opportunity to shape legal strategy at the intersection of health, fitness, and consumer products.
Fate Therapeutics is looking for an Executive Director or Senior Director in Regulatory Affairs to oversee and direct the strategic planning and execution of clinical regulatory activities essential for initiating and conducting clinical trials and securing regulatory approvals. Provide strong cross-functional leadership for global filings including authoring/reviewing sections of IND/CTA, NDA/BLA/MAA, and other global submission documents in support of clinical trials and marketing applications, as well as their amendments, in conformance with local regulatory requirements. Provide mentorship and oversight of Regulatory Affairs staff to plan, manage, author, coordinate, and review regulatory submission documents and development activities to support regulatory filings and dossier lifecycle. Qualifications BS/MS/PhD degree in a life science with at least 12 years of progressive experience in Regulatory Affairs in the biotechnology or pharmaceutical industry. Previous cell therapy product experience and regulatory knowledge is highly preferred.
This role is essential for managing patient registration, insurance verification, and specimen processing within a fast-paced, patient-centered environment.. Specimen Processing and Phlebotomy: Perform phlebotomy, process drop-off specimens, and conduct routine EKG tracings as required.. Patient Flow and Coordination: Assist in managing patient flow for ambulatory care, pre-op testing, and clinics.. Certified Phlebotomy Technician (CPT) preferred, but not required.. Preservatives for 24 hour urine/stool collection, x-ray developer and fixer solutions
Comprehensive medical coverage with low copay options, including prescription drug, behavioral health, and free telemedicine services.. Support for family planning through fertility benefits and adoption assistance.. Preferred certifications include RMA, CCMA, CMA, NCMA, or NCRMA.. HCA Healthcare is recognized as one of the most ethical companies globally, emphasizing our commitment to community care with significant charitable contributions.. - Dr. Thomas Frist, Sr., HCA Healthcare Co-Founder
We’re a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development.. This role requires experience with NDA/BLA, MAA and supplementary applications.. Bachelor's degree and at least 12 years industry experience with a minimum of 10 years direct Regulatory Affairs experience in the biotech/biopharmaceutical industry.. Experience in the successful prosecution of NDA/BLA, MAA and supplementary applications in essential.. Experience in managing the preparation of a marketing application (NDA/BLA/MAA) in CTD format for a major market (US, EU, Canada).
Aypa Power, a Blackstone portfolio company, is a leading developer, owner, and operator of utility-scale energy storage and hybrid renewable projects that power our communities and cities.. We have been at the forefront of energy storage development since our first energy storage project came online in 2018.. As a leader in our industry, we have over 22 GW of utility-scale energy storage and hybrid renewable energy projects in development and 33 projects in operation or construction across North America.. We are seeking a strategic and experienced Senior Director of Government & Regulatory Affairs to lead state and local engagement across key Midwest and Eastern markets, ensuring our portfolio of energy storage and hybrid renewable projects through evolving political, policy, and regulatory environments.. Monitor and influence legislative and regulatory proceedings impacting energy storage and project siting;
Unlike traditional cold-storage methods, the OCS Systems feature warm, normothermic perfusion, and provide the means to monitor organ health so that transplant patients can experience better outcomes. Prepare regulatory submissions for the FDA, including PMA and IDE applications, supplements and reports and 510(k) submissions.. Solid experience and proven track record in successful FDA submissions including IDE and PMA applications, supplements and reports. Director Global Regulatory Affairs - Precision Medicine and Digital Health.. Senior Director, Global Regulatory StrategySenior Director, Regulatory Affairs Advertising & PromotionSenior Director, Global Regulatory StrategyHead of Regulatory Affairs, Cell Therapy ImmunologySenior Manager / Associate Director, Regulatory Strategy - CMCDirector, Regulatory Affairs Advertising & Promotion
Perform these management and leadership duties while being responsive to constant change and revision of budget levels, accreditation, and accountability programs, economic changes, and the changing needs of the patient population and changing state of inpatient psychiatric treatment.. Oversight of treatment requirements : Ensure that the treatment and services provided to patients meet all regulatory requirements, including the Joint Commission, the Colorado Department of Public Health and Environment, the CDHS Behavioral Health Administration, and the Centers for Medicare and Medicaid Services.. Establish policies and procedures and methods of operation to ensure the existence of an effective performance improvement program; patient safety program, and risk management program within the hospital.. Assure balanced resource deployment (personnel services, operating, and capital outlay) between the Hospital's treatment programs, clinical departments and ancillary and support areas.. Conduct performance management and pay (PMAP) planning review and appraisal for direct reports.
Unlimited vacation , supportive parental leave policy, and company-wide holiday shutdown.. Key Responsibilities Lead and evolve Kepler’s global spectrum strategy, including frequency planning, global market access, ITU coordination, and other national or international licensing.. Secure and protect spectrum assets to support growth of Kepler’s LEO constellation, inter-satellite links, and future innovation in optical and lunar relay systems.. Required Skills & Qualifications 10+ years in spectrum management, regulatory affairs, or telecom law within the satellite or aerospace sector.. Technical expertise in RF engineering, satellite systems, and/or inter-satellite links.
Title: Senior Specialist, Compliance and Regulatory Affairs. Reports to: Senior Director, Risk and Compliance. Location: Alexandria, VA preferred/Remote eligible if outside the DC metro area. Federal and/or State Government Agencies Occasionally. Assist other team members with continuous improvement of compliance/qualifications assessment review processes and procedures
We believe that blockchain and digital asset innovation will transform how value moves through the world – and we're building the products and services to make that future a reality.. Our institutional digital assets platform spans trading, investment banking, asset management, staking, self-custody, and tokenization technology.. Led by CEO and Founder Michael Novogratz, our team blends deep crypto expertise with institutional experience and a shared commitment to shaping the future of Web3 and AI.. In addition to ensuring compliance, you will attend Independent System Operator ("ISO") or Public Utility Commission ("PUC") stakeholder meetings, workshops, and discussions to advocate for Galaxy's position within the relevant market.. Direct, recent experience within the ERCOT and PUCT stakeholder environment
The Associate Administrator of the community hospital serves as a key member of the senior leadership team, reports directly to the community hospital Chief Executive Officer.. As the Associate Administrator, this role works collaboratively with physicians, nursing and departmental leadership to achieve operational excellence in delivery of patient care usage of staffing and supply resources, and overall throughput of patients.. Leads planning and execution of growth opportunities to include community outreach and physician partnership development.. Masters degree in Healthcare Administration or equivalency is required.. A minimum of five years of progressive leadership experience in healthcare management, in a hospital setting is highly preferred.
Join to apply for the ASC Accreditations & Quality Manager role at Illinois Bone & Joint Institute.. Description ASC Ventures is currently seeking an ASC Accreditations & Quality Manager to oversee those aspects for our ambulatory surgery centers (ASCs).. Summary The ASC Accreditations & Quality Manager will ensure our ambulatory surgery centers meet the required standards of quality and safety, work in collaboration with site Administrators to implement standards from accreditation bodies including The Joint Commission, Accreditation Association for Ambulatory Health Care (AAAHC), and support Administrators in maintaining facility standards in accordance with all regulatory requirements and accreditation standards.. Requirements The ideal candidate will have proven progressive leadership experience in an ASC setting, possess expert-level knowledge of the accreditation standards, management of a multidisciplinary clinical team, and understanding of nursing practice and working with surgeon customers.. Certifications like Certified Professional in Healthcare Quality (CPHQ) are highly valued.
Subject matter expert in the area of Biologics.. Develop and Execute Global Regulatory Strategies: Formulate and lead global CMC and clinical regulatory strategies for Biologics, Biosimilars, and Small Molecules.. Lead and Manage Global Regulatory Submission Activities: Oversee submission planning, authoring, reviewing, and coordination for regulatory filings (e.g., BLA, MAA).. Health Authority Interactions and Negotiations: Initiate and lead Health Authority interactions, including preparing briefing books, planning rehearsals, and risk mitigation.. Assess regulatory impact of changes in CMC procedures and oversee internal regulatory guidance documents.