Collecting information
Organizing data
The Patient Care Coordinator is the first point of patient contact and requires professionalism, accuracy, and efficiency to ensure smooth front-office operations, proactive patient engagement, exceptional service, and effective coordination with clinical teams.. Schedule: 5, 8-hour shifts per week: Monday – Friday during open clinic hours (7:00 am – 5:00 pm). Maintain accurate records and update electronic health records (EHR) systems. Knowledge of insurance verification, medical terminology, and EHR systems preferred. We believe everyone–of every race, gender, sexuality, age, location, and income–deserves the opportunity to live their healthiest life.
We are advancing an innovative portfolio of therapeutics, drawing on leadership that previously played key roles in the design, development, and commercialization of cutting-edge targeted cancer therapies, including antibody-drug conjugate therapies (ADCs).. Serve as a subject matter expert on regulatory systems (e.g., Veeva Vault), overseeing system use in collaboration with IT and Quality, user training and data archiving.. 7+ years of experience in regulatory affairs with a strong emphasis on early-phase drug development.. Are you currently or have you ever been excluded or debarred by the OIG, DOJ, FDA, or any other Federal or State agency?. Do you have experience in regulatory affairs within Oncology with a strong emphasis on early-phase drug development?
Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences. The Senior Director, Regulatory Affairs is a strategic and operational leader responsible for overseeing regulatory strategy, execution, and compliance across all phases of drug development but with a primary focus on early-stage first-in-human / first-in-class molecules. The Senior Director will lead a team of Regulatory Affairs professionals and serve as the primary liaison with global health authorities, including the FDA, EMA, and Health Canada. Deep knowledge of Health Canada and FDA regulatory frameworks, including CTA and IND processes. Understanding of Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and Good Clinical Practice (GCP).
A Licensed Mental Health Therapist (LMHT) is a fully licensed professional providing mental health services at a Master’s level or above, often running or expanding a private practice.. Licensed Mental Health Therapist — Are you ready to launch or expand your private practice?. You’re a fully-licensed Mental Health Therapist at a Master’s level or above with LMHC, LPCMH, LIMHP, LMFT, LMFTS, LCMFT, LPC, LPCC, LCPC, LCPCS, LPCC-S, LCSW, LICSW, or LCSCW licensure (accepted on a state by state basis), a valid NPI number, and malpractice insurance.. Increase your earnings: Secure higher rates with top insurance plans through access to our nationwide insurance network.. Licensed Mental Health Therapist, Mental Health Counseling, Private Practice, Insurance Credentialing, Patient Care, Billing and Compliance, EHR Management, Medicare Advantage, Medicaid, Continuing Education
This unique opportunity is at a prestigious facility looking to hire a traveling therapist. This exciting area offers many recreational activities. As a premier travel therapy company, Host Healthcare offers top pay, excellent benefits, and personalized service. The ideal candidate for this position will be dedicated to providing patients with the highest level of service. The ideal candidate will also be knowledgeable in Medicare, Medicaid, and private insurance, as well as the ability to complete relevant insurance documentations.
The role involves providing direct patient care, collaborating with the healthcare team, and utilizing electronic health records (EHR). Utilizing electronic health records (EHR). Performing patient assessments, medication administration, and treatment planning (as applicable to the cardiology setting). Proficiency in electronic health record (EHR) systems (EPIC specified). Only candidates within a 50-mile radius or willing to relocate to Seattle and commit to a permanent position will be considered.
Virginia Mason Franciscan Health is seeking a dedicated Medical Staff Peer Review Specialist to support our medical staff in maintaining the highest standards of clinical excellence.. Virginia Mason Franciscan Health has a rich history of providing exceptional healthcare, dating back to 1891.. Building upon a legacy of compassionate care and innovation, our organization has evolved over the years through strategic partnerships and integrations to expand our reach and services across the Puget Sound area.. Today, as Virginia Mason Franciscan Health, we remain deeply committed to healing the whole person - body, mind, and spirit - in the communities we serve.. When you join Virginia Mason Franciscan Health, you become part of a team that delivers top-quality, professional healthcare in modern, well-equipped facilities, and contributes to a legacy of service built on collaboration and shared purpose.
The Quality Control Supervisor’s role is to administer corporate policies and procedures as they relate to quality and food safety, in conjunction with the QC Manager through performance, supervision, monitoring and development of quality systems and processes. Verify vendor compliance and monitor receipt, storage, and handling. Maintaining food safety and quality by reporting all food safety risks or quality issues to QA and plant management immediately, and holding all at-risk products for management review. HACCP and/or PCQI certification would be a plus. HACCP and/or PCQI Certification
Maxim Healthcare in Port Orchard is hiring for a Licensed Practical Nurse (LPN) to help support a Veteran in the comfort of their home.. Current TB or Chest X-Ray.. Medical/Prescription, Dental, Vision, Health Advocacy (company paid if enrolled Medical) and Health Advocate Employee Assistance Program. Health Savings Account, 401(k), Short Term Disability, Voluntary Group Life Insurance and Supplemental Accidental Insurance, Hospital Expense Protection Plan, Critical Illness Insurance, Home and Auto Insurance discounts, Pet Insurance and Legal Benefits. We offer private duty nursing, skilled nursing, physical rehabilitation, companion care, respite care and behavioral care for individuals with chronic and acute illnesses and disabilities.
At Parker Aerospace, we develop technologies and innovative solutions that enable reliable, efficient and increasingly sustainable flight for the lifecycle of the aircraft, including aftermarket support. At Exotic Metals Forming Division, our highly talented team blends a passion for manufacturing with relentless customer support, making us the partner of choice for complex aerospace solutions. That is why we are so proud of everyone in our Exotic family who strives to be the best at what they do every day, working as a collaborative team in a culture of continuous improvement to stretch the bounds of creative thinking and provide quality products to our customers around the globe. Come join the Parker Aerospace Team!. This position is subject to meeting U.S. export compliance and/or U.S Government contracting citizenship eligibility requirements.
Reports to: Quality Supervisor. Create, implement and verify the accuracy of standard process trees within material requirements planning (mrp) systems and to develop standard operating procedures (SOP's) to ensure process tree consistency and accuracy for like processes/approvals at each plant during the initial deployment of the mrp system.. Applied Learning - Ability to participate in needed learning activities in a way that makes the most of the learning experience.. Due to the manufacturing environment, Personal Protection Equipment may be required including safety glasses, goggles, aprons, rubber boots, gloves, and a respirator (provided by Company).. Please apply at Aerospace Metal Finishing Careers | Aerospace Jobs (valencesurfacetech.com) with up-to-date work history and contact information.
Automating tests using API and UI frameworks like Selenium, Java, and SOAP UI. 5-10 years of proven software test engineering experience in an Agile Development Environment. Expertise in Selenium, Java, and API/UI test automation. Strong knowledge of tools such as SOAP UI, JIRA, HP ALM, and experience with mobile application testing. Los Angeles County Fair Chance Ordinance for Employers
The Quality Assurance Manager reports to the Senior Director, Nuclear Quality and Continuous Improvement (QA&CI).. Experience with industry codes, standards and guides such as ASME, AWS, AISC, ASTM, EPRI, NEI, ISO, NEC and IEEE are strongly desired.. 12+ years' experience in a Quality Assurance function with 5+ years as a Manager in a nuclear (NRC, DOE) Quality Assurance function preferred or in a regulated environment such as, EPA, aerospace, or similar industries.. TerraPower must evaluate applicants who are foreign nationals (other than asylees, refugees, or lawful permanent residents) in accordance with U.S. Government export control requirements.. To facilitate TerraPower's export control reviews, you will be asked as part of the application process to identify whether you are a U.S. Citizen or national, asylee, refugee, or lawful permanent resident of the United States.
At Snoqualmie Valley Health, we're not just in the business of healthcare; we're in the business of empowering our community to live boldly and live well.. POSITION SUMMARY: The Inpatient Pharmacy Technician plays a key role in supporting pharmacy operations across a variety of responsibilities in our critical access hospital setting.. This position is responsible for sterile compounding (including IV preparation), medication delivery to patient care areas, inventory management, purchasing support, and assisting with 340B program audits and compliance.. Collaborate with pharmacists and nursing staff to optimize workflow and medication delivery systems. The COVID vaccine and flu shot (during flu season) are required for employment, with exemptions available for valid medical or religious reasons.
We are seeking a highly motivated and skilled Certified Nursing Assistant (CNA) to join our team in Seattle.. The CNA will be responsible for providing basic patient care under the supervision of the registered nurses in a fast-paced LTC environment.. As the nation’s first healthcare staffing company, Interim HealthCare Staffing has created a career path for CNAs that makes work-life balance achievable and rewarding.. Provide basic wound care and dressing changes as directed by the Registered Nurse. From home care and hospice services to healthcare staffing and specialized care, Interim HealthCare combines the resources of a national organization with a uniquely personal approach in each of our communities.
We provide outstanding telehealth services to patients throughout the United States.. Provide top-notch, patient-focused care.. Stay updated on the latest in telemedicine and clinical guidelines.. Board-certified in 1+ relevant medical specialties: Internal Medicine, Pediatrics, Family medicine, General Practice, Obstetrics, Gynecology, Dermatology, Cardiology, etc.. Nice to Have: Telemedicine/Telehealth/Virtual medical experience is preferred but not required.
Manager, Regulatory Affairs Aesthetics (Bothell, WA).. We are a global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes. We develop, manufacture and market a range of products, primarily in gastroenterology, hepatology, neurology, dermatology, medical aesthetic devices, international pharmaceuticals. Prepare and submit regulatory documents for post-market surveillance, including annual reports, and other required documents. Should have experience authoring complete 510(k) submissions, Medical Device license applications (Class II or above), EU MDR technical file dossier (Class II or above).
Senior Regulatory Affairs Associate. With a track record of global leadership in bone marrow transplantation, HIV/AIDS prevention, immunotherapy and COVID-19 vaccines, Fred Hutch has earned a reputation as one of the world's leading cancer, infectious disease and biomedical research centers.. Fred Hutch operates eight clinical care sites that provide medical oncology, infusion, radiation, proton therapy and related services, and network affiliations with hospitals in five states.. The Senior Regulatory Affairs Associate works with faculty and staff in the Infectious Disease Sciences (IDS) Program in the Vaccine and Infectious Disease Division to ensure all regulatory compliance measures are followed for clinical trials by coordinating regulatory submissions and monitoring as well as assisting with the resolution of compliance issues.. In partnership with the PI, prepare and track all clinical activity documents including IRB/IBC/site registration approvals, safety reports, deviations, laboratory certifications, staff training & licenses, monitoring notices and reports, inspections & compliance, etc.
Business Operations Lead - Verity (Senior Director)(Hybrid) page is loaded Business Operations Lead - Verity (Senior Director)(Hybrid) Apply remote type Hybrid locations Kirkland, WA time type Full time posted on Posted Yesterday job requisition id 25009884 We are seeking a strategic and execution-focused Business OperationsLead (Senior Director) to lead and scale our post-sales functions, including account management, implementation, training, analytics, and sales operations.. Support revenue growth through operational alignment with Sales, Marketing, and Customer Success.. Deep understanding of pharmacy operations, data, and regulatory considerations (e.g., PBMs, 340B, e-prescribing, medication adherence).. Bachelor’s degree in business, Healthcare Administration, or related field (MBA or PharmD preferred).. Evernorth Health Services, a division of The Cigna Group, creates pharmacy, care and benefit solutions to improve health and increase vitality.
Principal Regulatory Affairs Specialist. As a critical member of the Philips Ultrasound- Regulatory Affairs Organization, the Principal Regulatory Affairs Specialist will lead and provide regulatory oversight for critical new product development projects, ensuring our state-of-the-art Ultrasound Products meet FDA, and other governmental agency/notified body Regulatory Compliance standards/requirements.. You have strong knowledge of US FDA, China NMPA, CE Marking, EU MDD/MDR, JPAL, Canadian CMDCAS etc.. with proven/successful preparation and submission of Technical Documentation, 510(k), De Novo, PMA, and registrations of medical devices globally.. We are a health technology company.