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TravelNurseNetwork is working with Compunnel Healthcare to find a qualified Case Manager RN in Olympia, Washington, 98506!. Case Management/Utilization Review. DRG (Diagnosis Related Groups). Ambulatory Healthcare Facilities, Acute Care and Teaching Hospitals, Health Systems, Laboratories, Pharmaceutical Companies, Medical Device Companies, Clinical Research Organizations, Private Physician Practices, Long and Short-Term care, Health Insurance Companies, and MORE!. Nursing, Allied Health, Healthcare Administrative, Biomedical, Pharmaceutical and more, just ask us!
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).
Where Kids and Families are Always First MultiCare Mary Bridge Children’s Hospital is the state-designated Level II Pediatric Trauma Center and the only pediatric hospital in Washington’s South Sound Region dedicated to a comprehensive network of health services for children and adolescents.. Mary Bridge Children’s multi-disciplinary approach to care includes pediatric experts for emergency services, inpatient care, and outpatient specialty clinics, all specializing in kids and their unique needs.. Weekends and eveningsPosition SummaryThe Patient Care Technician is an ideal opportunity for those seeking a dynamic and comprehensive role within our health care system.. Collaborate with health care practitioner or registered nurse for comprehensive quality care Requirements. orgPay and Benefit ExpectationsWe provide a comprehensive benefits package, including competitive salary, medical, dental and retirement benefits and paid time off.
pay in the industry• Weekly paychecks• Comprehensive malpractice insurance• Workers compensation insurance, etc.. Serene Nursing Services, LLC is an Equal Opportunity EmployerRequirementsResponsibilities: - Provide direct patient care under the supervision of a Certified Medical Assistant or Licensed Practical Nurse or registered nurse.. - Monitor and record vital signs, such as blood pressure, temperature, and pulse.. - Assist with mobility and transfers, ensuring patient safety.. - Follow aseptic techniques to prevent infection and maintain a clean and safe environment.
Radiant Medical Staffing is a leading providerof healthcare staffing solutions.. We are dedicated to connecting skilledprofessionals with top-tier facilities to ensure quality patient care.. As an Occupational Therapist, you will be responsible for assessing patients' needs and developing individualized treatment plans to help them achieve their therapeutic goals.. Familiarity with electronic health records (EHR) systems. Certification in specialized areas of practice (e.g., pediatrics, geriatrics, hand therapy)
destinationone Consulting specializes in recruitment across diverse sectors, including Healthcare, Health Tech, Government, Municipalities, Non-Profits, Legal, Public Accounting, Food and more.. The Quality Assurance Coordinator is responsible for monitoring and evaluating the quality of care provided within the healthcare practice, ensuring that standards are met and continuously improved.. Bachelor's degree in Healthcare Administration, Nursing, or a related field; certification in quality management preferred.. Experience in quality assurance or improvement in a healthcare setting.. Disclaimer: We're proactively building a databank for opportunities in Healthcare, Health Tech, Government, Non-Profits, Legal, and more.
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.
Here is your opportunity to get your foot in the door as a state worker!. We are now accepting applications for our on-call Nursing Assistant Certified position at the historic Washington Soldiers Home in Orting, Washington!. These locations provide Medicare and Medicaid nursing home care to Veterans, including, in some instances, their spouses, widows, or Gold Star Families.. If you are a nursing assistant with a passion for excellence and compassionate care, we invite you to be a part of our team at the Washington Soldiers Home by applying today!. Requires medical evaluation, fit testing, training, and use of respiratory protection as required by the Washington Industrial Safety and Act standards.
This position requires deep understanding of all aspects of the drug development process from early clinical stages to post commercialization; with emphasis on the large global clinical trials and regulatory filing activities.. A clinician (M.D., or D.O.) preferably a psychiatrist or neurologist including prior management experience (direct or indirect).. Requires thorough knowledge of clinical medicine and/or clinical pharmacology and associated disciplines (e.g. biostatistics, data management, medical writing).. Advanced understanding of drug development principles and clinical trial implementation and management.. If you believe you are the victim of fraud resulting from a job recruiting scam, please contact the FBI through the Internet Crime Complaint Center at: , or your local authorities.
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.
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.. Bachelors degree in life sciences, pharmacy, or related field; advanced degree (PhD, PharmD, MS) preferred.. 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?
Northwest Medical Specialties, PLLC, is a leading Hematology/Oncology practice seeking a motivated, energetic, and compassionate physician to join our team.. The NWMS Hematologist/Oncologist specializes in the diagnosis, treatment, and management of both solid tumors and hematologic malignancies, including leukemia, lymphoma, myeloma, and other hematologic malignancies.. Working in a multidisciplinary healthcare environment, this physician provides expert care to patients, utilizing advanced diagnostic techniques, chemotherapy, immunotherapy, cellular therapy, and stem cell transplantation.. We are specifically seeking a candidate with expertise and or interest in cellular therapy, bispecifics, and CAR-T cell therapy.. Additionally, the hematologist/oncologist plays a critical role in educating patients and their families about disease management, treatment options, and expected outcomes.
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)
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).
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.
Collaborating with local sales and clinical counterparts and field-based reimbursement specialist team members to identify and deliver solutions that meet customer needs. MBA or Master's in Business, Hospital Administration, Nursing, or Life Science. Healthcare marketing or consultative selling experience in medical devices, pharmaceuticals highly desired. This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).. If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
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.
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.
This role requires a deep understanding of Medicaid programs, the regulatory environment, and the unique challenges of populations (i.e. TANF, ABD, DSNP, Foster Care, and DD/IDD).. Master’s degree (MBA, MPH, MPA) in business, public policy, or healthcare administration. 7+ years in business development and Medicaid procurements, particularly with complex populations (e.g., DD/IDD, Foster Care, Dual-Eligible Members)
Verathon, a subsidiary of Roper Technologies, is headquartered in Bothell, Washington, USA and has international subsidiaries in Canada, Europe and Asia Pacific.. Verathon is looking for a Director, Regulatory Affairs to become the newest member of our QA/RA Team located in Bothell, WA. This is an onsite position based in our Bothell WA Headquarters.. The Director, Regulatory Affairs is responsible for managing regulatory strategies for worldwide device and registration of Verathon products, in accordance with product development and business objectives.. Lead, mentor, and develop a team of Regulatory Affairs professionals and contracted clinical study, medical professionals, and other consultants. 8+ years experience in regulatory affairs within a regulated industry (e.g., medical devices, pharmaceuticals, biotechnology, or healthcare products)