Gastroenterologist Hospitalist Physician CommonSpirit HealthGastroenterologist Hospitalist PhysicianLakewood, WAOur integrated health system has nearly 1,500 hospital beds including Bailey-Boushay House, the first skilled-nursing and outpatient chronic care management program in the United States designed specifically to meet the needs of people with HIV/AIDS; Benaroya Research Institute, internationally recognized for autoimmune disease research; and Virginia Mason Institute, a teaching organization which coaches health care professionals and others around the world in the Virginia Mason Production System, an innovative management method for improving quality and safety. The center is founded on providing the best possible clinical outcomes to the patients it serves with additional focus on innovation through research as well as training the next generation of experts and leaders in the field.
Clinical Research Coordinator I MultiCare Health SystemClinical Research Coordinator ITacoma, WAFull timeThis position requires interaction with a wide variety of internal and external groups to include nursing staff, management, physicians, patients, outside organizations, research groups and service groups such as laboratories, pharmacy and radiology. The Clinical Research Coordinator I is responsible for the implementation of clinical studies, typically basic science, phase II, III, and IV trials, and IIR studies.
Clinical Research Assistant II MultiCare Health SystemClinical Research Assistant IITacoma, WAPart timeMinimum two (2) years of related experience in healthcare or research (bench research, clinical research or health services research) OR one (1) year of healthcare experience plus one year of industry related research experience within a healthcare setting (such as working for MIRI). If your purpose and passions align with ours, you'll find a place to grow, do meaningful work and build a career you love in a community that feels like home.
Clinical Research Assistant - Lacey Providence St. Joseph HealthClinical Research Assistant - LaceyLacey, WAPart timeOur not-for-profit network also provides a full spectrum of care with leading-edge diagnostics and treatment, outpatient health centers, physician groups and clinics, numerous outreach programs, and hospice and home care. Coursework/Training: Graduate of an accredited school for medical assistants, or an equivalent combination of coursework and experience/training sufficient to qualify to sit for the Washington State Certification exam.
Clinical Research Coordinator II - Madigan AMC The Henry M. Jackson FoundationClinical Research Coordinator II - Madigan AMCTacoma, WAFull timeHowever, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. Employment with HJF is contingent upon successful completion of a background check, which may include, but is not limited to, contacting your professional references, verification of previous employment, education and credentials, a criminal background check, and a department of motor vehicle (DMV) check if applicable.
Research Support Pharmacist MultiCare Health SystemResearch Support PharmacistTacoma, WAFull timeHome to the MultiCare Regional Cancer Center, a Family Birth Center and specialized neonatal care in partnership with Mary Bridge Children's, our collaborative, mission-driven teams offer a rewarding environment for career growth and professional excellence. Deliver training for pharmacists, technicians, study teams, and patients as needed; serve as a subjectmatter resource for investigational medication use across clinical areas.
Clinical Documentation Specialist for Professional Billing (PB) MultiCare Health SystemClinical Documentation Specialist for Professional Billing (PB)Tacoma, WAFull timeThe Clinical Documentation Specialist for Professional Billing (PB) conducts billing integrity reviews/audits, including reviewing billing submitted with all supporting clinical documentation to assess the extent to which applicable documentation and coding criteria have been met and to identify clinical documentation improvement opportunities. This position will work remotely but primary residence cannot be located in the following states:California, Connecticut, Florida, Hawaii, Illinois, Louisiana, Maryland/Washington DC, Massachusetts, Missouri, New Jersey, New York, Pennsylvania, and Vermont.
Clinical Director - Seattle and Portland Kidney Centers North West Kidney CentersClinical Director - Seattle and Portland Kidney CentersSeaTac, WAFull timeThe position is responsible for unit administration, long and short-range planning, program development, contributing to the overall NKC corporate administrative management as well as participating in the overall operations management of the Northwest Kidney Centers; supervising and personnel functions within the region; working with Medical Directors of the units and assisting the CNO with various committees and other assignments as deemed necessary and useful to the organization. This includes oversight responsibilities for the delivery of quality dialysis care to our patients, supervision of nurse managers, education of new clinical staff, development of cost-effective, innovative, high-quality services, and developing and monitoring budgets within established guidelines.
Clinical RFP Coordinator Cambia Health SolutionsClinical RFP CoordinatorTumwater, WAFull timeAs a member of the Clinical Program Management team, the Clinical RFP Coordinator & Communications Specialist partners with the Marketing and Sales teams by representing clinical areas of the company in business acquisition and retention opportunities. * Facilitates responses to RFPs, RFIs, and surveys for clinical areas in collaboration with sales bid response teams and other divisions to ensure timely delivery of high-quality responses.
Clinical Research Associate/Senior Clinical Research Associate- FSP ParexelClinical Research Associate/Senior Clinical Research Associate- FSPOlympia, WAFollows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance issues to Local Management and/or Clinical Quality Management (CQM) as required. The CRA is responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies, in compliance with Client Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies.
Senior Clinical Research Associate - CNS/Psychiatry - West Coast - Remote Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - CNS/Psychiatry - West Coast - RemoteWARemote$97,000–$193,000 / yearTypically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.
Senior Clinical Research Associate/Clinical Research Associate - All US Locations - FSP ParexelSenior Clinical Research Associate/Clinical Research Associate - All US Locations - FSPOlympia, WAFollows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance issues to Local Management and/or Clinical Quality Management (CQM) as required. The CRA is responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies, in compliance with Client Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies.
Clinical Research Associate II/Senior Clinical Research Associate - All US Locations - HEM/ONC - FS ParexelClinical Research Associate II/Senior Clinical Research Associate - All US Locations - HEM/ONC - FSOlympia, WAWork in partnership with and/or escalate to the SCP to ensure quality of site delivery + Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites + Partner with Site Care Partner to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients; provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks + Attend investigator meeting when required (virtual or F2F). The CRA is responsible for the resolution of all protocol-related issues for assigned investigator sites and will work closely with the Site Care Partner (SCP), and other members of the study team, as required, in activities associated with the set-up, running and close-out of sites in a clinical trial.
Clinical Research Coordinator II Iterative Scopes IncClinical Research Coordinator IITacoma, WABy combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies.
Clinical Director, Clinical Research, Ophthalmology MerckClinical Director, Clinical Research, OphthalmologyOlympia, WA$255,800–$402,700 / yearJob Responsibilities** + Specifically, the Clinical Director may be responsible for: + Planning clinical trials (designing, collaborating on operational plans, etc.) based on the clinical development strategy + Medical oversight and overall conduct of ongoing or new clinical trials for investigational or marketed drugs + Analyzing and summarizing clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication + Participating in internal and joint internal/external research project teams relevant to the development of new compounds, and the further study of marketed compounds + Supporting business development assessments of external opportunities The Clinical Director may: + Actively engage with other functional areas in support of study execution + Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and + Assist the team in ensuring that other colleagues are informed of the progress of studies of our company and competitors' drugs, and + Provide expert opinion, internally and externally, on relevant scientific questions within their responsibility. The Clinical Director is responsible for maintaining a strong scientific fund of knowledge by: + Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies + Identifying scientifically and operationally strong investigators who can assist in the development of our company's investigational and marketed drugs + Establishing communications with prominent clinical investigators in his/her particular field of interest, particularly those who will be willing and able to assist in the evaluation of our company's drugs + Attending appropriate scientific meetings to maintain his or her competency and to maintain awareness of research activities in his/her area of responsibility.
Clinical Research Coordinator II Metis FoundationClinical Research Coordinator IIJoint Base Lewis-McChord, WA$60,000–$70,000The overall purpose of this study is to conduct, in collaboration with multiple Defense Health Agency sites and external collaborators, the development of a biosensor that will eventually be capable of integrating into a system comprising biosensors, respiratory risk assessment software, and healthy building controls to mitigate bioaerosol-related respiratory illnesses in military healthcare facilities. Assist relevant team members with the coordination of regulatory requirements such as protocol amendments, reportable events, writing informed consent forms and HIPAA forms, writing annual reports and IRB continuing reviews, and address stipulations issued from IRB to reach approval, while keeping investigators apprised of changes.
Clinical Research Assistant - Lacey Providence Health & ServicesClinical Research Assistant - LaceyLacey, WARequsition ID: 429122 Company: Providence Jobs Job Category: Research Job Function: Clinical Support Job Schedule: Part time Job Shift: Day Career Track: Clinical Support Department: 3033 WA PCH MEDICAL RESEARCH PROJECTS Address: WA Lacey 4525 Third Ave SE Work Location: PRCS Lacey-Lacey Workplace Type: On-site Pay Range: $22.44 - $34.33 Responsibilities include coordinating study timelines and resources, ensuring accurate collection and submission of research data to sponsors, and supporting regulatory compliance through informed consent preparation, regulatory documentation, adverse event and protocol deviation reporting, and continuing review activities.
Physician - Neurobehaviorialist MultiCare Health SystemPhysician - NeurobehaviorialistTacoma, WAFull timeThis physician provides comprehensive outpatient assessment and long-term management for individuals with conditions such as Alzheimer's disease, frontotemporal dementia, vascular cognitive impairment, and other neurodegenerative or neuropsychiatric syndromes. The position supports the diagnosis and continuum of care for neurobehavioral disorders, utilizing advanced neuroimaging, cognitive testing, and pharmacological as well as non-pharmacological interventions.
Pediatric Audiologist MultiCare Health SystemPediatric AudiologistTacoma, WAFull timeThe Audiologist provides specialized comprehensive diagnostic and rehabilitative services to a diverse linguistic, ethnic, cultural, and socioeconomic group of pediatric patients age birth to 21 years in medical center/clinical setting. The Audiologist serves a large population of patients with multiple disabilities and maintains both internal and external contacts including patient care staff, physicians, and support staff.
Security Officer MultiCare Health SystemSecurity OfficerTacoma, WAFull timeMultiCare 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. Award-winning:Named 'Top Children's Hospital' for five years by the Leapfrog Group; physicians consistently named on 'Top Doctors' lists by Seattle Magazine, Seattle Met and the Tacoma News Tribune.
Senior Medical Director, Clinical Research Neurology Sumitomo PharmaSenior Medical Director, Clinical Research NeurologyOlympia, WA$284,320–$355,400 / yearSumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. **Our** **Mission** _To broadly contribute to society through value creation based on innovative research and development activities for the betterment of healthcare and fuller lives of people_ _worldwide_ **Our** **Vision** _For Longer and Healthier Lives, we unlock the future with cutting edge technology and_ _ideas_
Research Fellow, Medical Device Toxicologist Bausch + LombResearch Fellow, Medical Device ToxicologistOlympia, WA$150,000–$200,000 / yearThe Research Fellow - Medical Device Toxicologist will provide cross functional Preclinical medical device expertise supporting internal and external stakeholders pertaining to biocompatibility and associated focus areas, for medical device development, product expansion and maintenance. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe.
Sr. Clinical Trials Manager Agilent Technologies IncSr. Clinical Trials ManagerWAMonitor and review study budget and data management activities, such as PRF development, training, and facilitating query resolution with proper documentation • Support monitoring efforts by setting quality and compliance goals by overseeing and approving study monitoring plans, may review, suggest edits and approve monitoring trip reports • Contribute to contract review and negotiations with outside vendors and study sites or laboratories • Mentor CTMs and CRAs • Demonstrate an ability to influence others to achieve positive results and collaboration through diplomacy and respect for others, appropriate prioritization and facilitation of the decision-making process Qualifications Qualifications: • Bachelors degree or higher, or equivalent credentials • Knowledge of GCP, ICH guidelines, and other clinical regulatory requirements • Strong interpersonal skills (verbal and written), organizational, and prioritization skills, able to communicate at multiple levels of an organization and with sponsors/clients. Primary Responsibilities (all levels): • Manage, design and implement all clinical operational aspects of IVD clinical trials from inception through close-out • Serve as main point of contact for internal and external study stakeholders; effectively communicating, collaborating, managing escalation of issues, where necessary, as well as participating and leading internal and external study meetings • Identify, evaluate, and oversee qualification and contracting for study investigators, study sites, CRO and/or vendor management for the study, where applicable • Develop or assist in the development of study-related plans and documents including protocols, informed consent forms, monitoring plans, case report forms, training plans and engagement materials • Ensure trial master file (TMF/eTMF) is established, current, and maintained per ICH E6.
Research Scientist- Remote Community Health Center IncResearch Scientist- RemoteWARemoteThe system delivers primary care to more than 150,000 patients in Connecticut, and extends access to specialty care for more than 2.5 million individuals across the U.S. It is a national accrediting body for organizations training advanced practice providers, and offers accredited education and training for Medical Assistants in multiple states. As an incubator for new ideas in areas including social justice, the environment, and social determinants of health, the MWHS is addressing challenges faced by providers caring for underserved communities, creating innovative and impactful initiatives led by nationally and internationally recognized experts.
Research Fellow, Pharma Toxicology Bausch + LombResearch Fellow, Pharma ToxicologyOlympia, WA$150,000–$200,000 / yearThe Research Fellow, Pharma Toxicology, will provide comprehensive, cross functional preclinical expertise to internal and external stakeholders, with a focus on toxicology, and related scientific disciplines that support pharmaceutical development, and ongoing lifecycle management. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe.
Spanish Bilingual Registered Dietician Clinical Trials Telehealth - Per Diem - Washington IQVIASpanish Bilingual Registered Dietician Clinical Trials Telehealth - Per Diem - WashingtonTacoma, WARemoteKey Responsibilities** As a Remote Registered Dietitian, you will: + Conduct nutritional assessments via telehealth and develop individualized dietetic care plans for patients with varying disease classifications + Provide ongoing dietary counseling and education to patients and their families + Deliver nutrition services **only to patients in states where you are licensed to practice** + Support patients enrolled in clinical research studies by monitoring nutritional progress and adherence + Maintain accurate, timely, and confidential clinical documentation + Participate in virtual team meetings, training sessions, and study-related activities **Qualifications** + Credentialed **Registered Dietitian (CDR)** with current national registration + Active, unrestricted **state licensure** (except CA, MI, NJ, AZ, VA, and CO) + Minimum **1 year of experience** providing nutrition planning and patient coaching + Minimum **1 year of experience delivering care remotely** via telehealth + Strong communication and interpersonal skills + Experience working with patients with obesity, with or without diabetes (preferred) + Experience managing patients on **GLP-1 therapies** (preferred) + **Spanish-English bilingual proficiency is required.** **Why Join IQVIA?** + Flexible per diem schedule that fits your lifestyle + Opportunity to gain exposure to clinical trials and research-focused care + Competitive supplemental income + Be part of a global organization advancing innovation and patient outcomes **Additional Information** + This position is **not eligible for visa sponsorship** . \#LI-CES and #LI-DNP #LI-HCP #remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
NewResearch Intern Iterative HealthResearch InternTacoma, WAAssist with managing recruitment and referral networks, screening subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant's eligibility or exclusion and prioritizing patients for outreach and follow up. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need.
Clinical Trial Associate Eliassen GroupClinical Trial AssociateOlympia, WA$37–$40 / hourClinical Trial Associate** **Anywhere** **Type:** Consulting **Category:** Clinical Ops **Industry:** Life Sciences **Workplace Type:** Remote **Reference ID:** JN -062026-107240 **Date Posted:** 06/02/2026 **Shortcut:** http://careers.eliassen.com/Cf1whs + Description + Recommended Jobs **Description:** _Remote_ Our client seeks a Clinical Trial Associate to support clinical trial coordination activities across assigned studies. + Collaborate with Clinical Data Management and Digital Informatics to enable timely training and system access for external stakeholders, including CRO and site staff, across platforms such as EDC, IWRS, ePRO, and eTMF.
Director, Global Clinical Development Otsuka America Pharmaceutical Inc.Director, Global Clinical DevelopmentOlympia, WADetailed Description of Duties:** - Otsuka is seeking a Director, Global Clinical Development (GCD) based Remotely or in our Princeton, NJ or Rockville, MD offices, who will be responsible for the design and oversight of clinical research programs and protocols for OPDC products under good clinical practices (GCP). Minimum $209,599.00 - Maximum $313,375.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States.
Research Principal, Real World Evidence CytelResearch Principal, Real World EvidenceOlympia, WASubject matter expertise in causal inference methods for comparative effectiveness studies, including target trial emulation, and/or developing real-world external control arms for clinical trials + Extensive experience with large healthcare real-world databases (electronic health records, claims databases) + Strong programming in R + Experience, vision, creativity, scope, integrity, leadership skills, prestige and intellect to enhance the existing organization and constructively contribute to the strategic direction of Cytel. Responsible for junior staff meeting the technical aspects their career development goals + Leadership or significant contributions to scientific processes involved with client deliverables (e.g., report templates, analysis plans, development of internal software/tools) + Can identify independently relevant methods, techniques and evaluation criteria for obtaining results + Keep abreast with regulatory, reimbursement and other industry requirements and guidelines, including via active participation in scientific conferences and symposia.
Project Leadership - Mid/Large- (clinical trials) - Homebased - (future needs) ParexelProject Leadership - Mid/Large- (clinical trials) - Homebased - (future needs)Olympia, WAIndividuals selected for these roles will provide leadership to project teams and manage the day-to-day operations while striving to achieve operational excellence through on time delivery within budget and to the highest quality with the goal to exceed client expectations Successful candidates possess an undergraduate degree in a clinical or health related field: advanced degree preferred, along with a minimum, 2+ years' experience leading Global Clinical Trials in Project Management within a CRO (preferred), Biotech or Pharma company. The Global Project Leadership department has dedicated members at all levels who are aligned to work with specific types of clients and deliver solutions customized to fit those client's needs, working on projects spanning across all phases of global clinical trials, in a wide array of therapeutic areas.
DSHS BHHA WSH Research Investigator 2 State of WashingtonDSHS BHHA WSH Research Investigator 2Lakewood, WA$73,284–$98,520 / yearThe incumbent may be required to perform the following during a recognized emergency/disaster: Report for duty on short notice for a specified timeframe; Report for duty outside of normally scheduled work hours and workdays; Report to a duty station that is different from the official duty station; Perform work task outside the normal scope of duties reflected in the Position Description Form. DSHS BHHA WSH - Research Investigator 2. Join the Research, Evaluation, and Data Analysis (REDA) Office at Western State Hospital as a Research Investigator 2. REDA is a collaborative analytics team that partners with clinical, operational, and executive leaders across the hospital.
Mgr Medical Affairs - Clinical Scientist Canon USA & AffiliatesMgr Medical Affairs - Clinical ScientistOlympia, WA$112,000–$203,000 / yearClinical Research and Validation** + Manage collaborative research and clinical evaluation projects at collaboration/partner sites including data collection, protocol development, data acquisition, phantom studies, equipment evaluations, post processing, co-writing papers, IP and technology transfer support, and development of presentations. **Mgr Medical Affairs - Clinical Scientist - req1715** **OVERVIEW** Work as part of a dynamic and fast-paced team of clinical and technical experts dedicated to positively impacting clinical care by effectively translating innovative imaging solutions to the clinical environment.
Endoscopy Associate Clinical Specialist (Upstate NY- Buffalo/Rochester) FujifilmEndoscopy Associate Clinical Specialist (Upstate NY- Buffalo/Rochester)Olympia, WAServe as a clinical liaison by developing and delivering comprehensive weekly and monthly reports to senior management that details installation and usage progress/metrics, staff training needs and effectiveness of completed training, and identifying trends to inform and strengthen KOL (Key Opinion Leader) relationships that support strategic decision making. Visit: https://www.fujifilm.com/us/en/about/region/careers **Job Description** **Duties and Responsibilities:** + Serve as the primary resource by providing continuous training and education of Fujifilm's equipment and/or services for our regional based customers.
Endoscopy Associate Clinical Specialist (Southern California - For Kaiser Permanent) NO RELOCATION FujifilmEndoscopy Associate Clinical Specialist (Southern California - For Kaiser Permanent) NO RELOCATIONOlympia, WAServe as a clinical liaison by developing and delivering comprehensive weekly and monthly reports to senior management that details installation and usage progress/metrics, staff training needs and effectiveness of completed training, and identifying trends to inform and strengthen KOL (Key Opinion Leader) relationships that support strategic decision making. Visit: https://www.fujifilm.com/us/en/about/region/careers **Job Description** **Duties and Responsibilities:** + Serve as the primary resource by providing continuous training and education of Fujifilm's equipment and/or services for our regional based customers.
Project Leadership - Biotech (clinical trials) -Dermatology - Home Based - (Future Needs) ParexelProject Leadership - Biotech (clinical trials) -Dermatology - Home Based - (Future Needs)Olympia, WAIndividuals selected for these roles will provide leadership to project teams and manage the day-to-day operations while striving to achieve operational excellence through on time delivery within budget and to the highest quality with the goal to exceed client expectations Successful candidates possess an undergraduate degree in a clinical or health related field: advanced degree preferred, along with at minimum, 2+ years' experience leading Global Clinal Trials in Project Management within a CRO (preferred), Biotech or Pharma company. **Parexel has upcoming opportunities at the Project Leader (PM) and Senior Project Leader (SPM) level for candidates with experience leading global studies in a variety of therapeutics including Dermatology, Respiratory, Neurology, Cardio, Oncology/ Hematology and GLP-1/Obesity.**
Clinical Psychologist - Autism Center (Federal Way) Seattle Children's HospitalClinical Psychologist - Autism Center (Federal Way)Federal Way, WashingtonTogether, we deliver superior patient care, advance new discoveries and treatments through pediatric research, and serve as the pediatric and adolescent, academic medical center for Washington, Alaska, Montana and Idaho – the largest region of any children’s hospital in the country. Prior to start of employment, must obtain, and maintain in good standing, medical or allied health professional staff privileges that are not limited, revoked, suspended, conditioned, or probationary, except for normal probationary periods due to initial appointment.
Research Analyst - Medical Management, Remote Providence Health & ServicesResearch Analyst - Medical Management, RemoteWashington, WARemoteRequsition ID: 438169 Company: Providence Jobs Job Category: Research Job Function: Clinical Support Job Schedule: Full time Job Shift: Day Career Track: Clinical Professional Department: 5018 HCS MEDICAL MANAGEMENT OR REGION Address: OR Portland 4400 NE Halsey St Work Location: Providence Health Plaza (HR) Bldg 1-Portland Workplace Type: Remote Pay Range: $See Posting - $See Posting The amounts listed are the base pay range; additional compensation may be available for this role, such as shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities. Providence Shared Services is a service line within Providence that provides a variety of functional and system support services for our family of organizations across Alaska, California, Montana, New Mexico, Oregon, Texas and Washington.
National Clinical Specialist Advanced Therapeutic FujifilmNational Clinical Specialist Advanced TherapeuticOlympia, WAThis role acts as a subject matter expert, bringing deep clinical and product knowledge in these specialized areas, and works closely with key opinion leaders (KOLs), customers, and internal teams-including sales management, product marketing, and field service engineers-to execute company initiatives. + Excellent written and oral communication skills, to articulate complex technical information clearly and concisely, present information to various groups of people, write reports and communicate associated information, and ensure effective collaboration with internal and external stakeholders across all levels of the organization.
Clinical Laboratory Scientist U.S. Department of DefenseClinical Laboratory ScientistTacoma, WA$69,373–$90,190 / yearA bachelors or graduate/higher level degree from an accredited college/university that included 16 semester hours (24 quarter hours) of biological science (with one semester in microbiology), 16 semester hours (24 quarter hours) of chemistry (with one semester in organic or biochemistry), one semester (one quarter) of mathematics, AND five years of full time acceptable clinical laboratory experience in Blood Banking, Chemistry, Hematology, microbiology, Immunology and Urinalysis/Body Fluids. Basic Requirement for Clinical Laboratory Scientist: Bachelors or graduate/higher level degree from a regionally accredited college/university including courses in biological science, chemistry and mathematics, AND successful completion of a Medical Laboratory Scientist/Clinical Laboratory Scientist program accredited by the National Accrediting Agency for Clinical Laboratory Sciences (NAACLS) or an accrediting body recognized by the U.S. Department of Education at the time the degree was obtained.
Assoc Clinical Spec (Regional) (Location: Baltimore or DC area - no relocation) FujifilmAssoc Clinical Spec (Regional) (Location: Baltimore or DC area - no relocation)Olympia, WAServe as a clinical liaison by developing and delivering comprehensive weekly and monthly reports to senior management that details installation and usage progress/metrics, staff training needs and effectiveness of completed training, and identifying trends to inform and strengthen KOL (Key Opinion Leader) relationships that support strategic decision making. Visit: https://www.fujifilm.com/us/en/about/region/careers **Job Description** **Duties and responsibilities** - Serve as the primary resource by providing continuous training and education of Fujifilm's equipment and/or services for our regional based customers.
Assoc Clinical Spec (Regional) (Location: Detroit or Ann Arbor Michigan) FujifilmAssoc Clinical Spec (Regional) (Location: Detroit or Ann Arbor Michigan)Olympia, WARemoteServe as a clinical liaison by developing and delivering comprehensive weekly and monthly reports to senior management that details installation and usage progress/metrics, staff training needs and effectiveness of completed training, and identifying trends to inform and strengthen KOL (Key Opinion Leader) relationships that support strategic decision making. Visit: https://www.fujifilm.com/us/en/about/region/careers **Job Description** **Duties and responsibilities** - Serve as the primary resource by providing continuous training and education of Fujifilm's equipment and/or services for our regional based customers.
Oracle Life Sciences Sr. Research Consultant- Epidemiology/Oncology OracleOracle Life Sciences Sr. Research Consultant- Epidemiology/OncologyOlympia, WA$31.83–$63.65 / hourAs a vital member of our team, you will contribute to research, analytics, and report writing for our syndicated products, as well as participate in custom oncology epidemiology consulting projects and client support Qualifications & Experience + Advanced degree in epidemiology field of study, preferable MPH (Master of Public Health) or Doctorate in Epidemiology. Oracle maintains broad salary ranges for its roles in order to account for variations in knowledge, skills, experience, market conditions and locations, as well as reflect Oracle's differing products, industries and lines of business.
Senior Director, Clinical Endpoint Adjudication Services CytelSenior Director, Clinical Endpoint Adjudication ServicesOlympia, WAThe Senior Director, Clinical Endpoint Adjudication Services is a strategic and operational leader responsible for the delivery, quality, and growth of endpoint adjudication services within Axio. This role ensures the design and execution of independent, blinded, and regulatory-compliant adjudication processes meet sponsor expectations and support high-quality regulatory submissions.
Clinical Instr/Asst/Assoc Professor of Nursing - Tacoma Campus Pacific Lutheran UniversityClinical Instr/Asst/Assoc Professor of Nursing - Tacoma CampusTacoma, WAOffering distinctive opportunities for global engagement, collaborative student-faculty research, and purposeful learning, our faculty guide 2,700 students from all faiths and backgrounds to discern their purpose through relevant coursework, inclusive mentoring, and internships at world-class Puget Sound-area businesses and institutions. Posting Number: 0603038 Recruitment Type: Open to All Applicants Position Title: Clinical Instr/Asst/Assoc Professor of Nursing - Tacoma Campus Position Type: Faculty Benefits Status: Benefits Eligible FLSA: Exempt Hiring Range: $108,000 per year for MSN prepared; $128,000 per year for Doctoral prepared and benefits package.
Oncology Clinical Consultant OracleOncology Clinical ConsultantOlympia, WA$79,100–$158,200 / yearBasic Qualifications** + Bachelor's degree in nursing + At least 8 years of total combined related work experience and completed higher education, including: + At least 5-years licensed health care practice + A minimum of 3 years Oncology/Hematology clinical experience + At least 1- year clinical consulting and/or other clinical healthcare information technology (HCIT) work experience + Professional license required: Registered Nurse - State Board + Work in accordance with corporate and organizational security policies and procedures, understand personal role in safeguarding corporate and client assets, and take appropriate action to prevent and report any compromises of security within scope of position. Utilizing effective consulting skills during project events, the Clinical Consultant will coordinate integration of clinical activities and workflow reviews, facilitate business process change and provide change management consulting to ensure that organizational aspects are addressed as new enabling technologies are implemented.
RN Clinical Consultant Guardian LifeRN Clinical ConsultantOlympia, WA$68,970–$113,310 / yearYou have** + A minimum of 5 years in direct patient care settings + BSN and CCM preferred + Excellent verbal and written communication skills and presentation skills + Ability to exercise independent & sound judgment in decision making + Strong problem-solving, analytical, clinical, and information research skills + Excellent time management & organizational skills + Demonstrated ability to multi-task with the ability to manage continually changing priorities and the ability to prioritize work based on customer service needs and departmental regulations + The ability to remain flexible due to changing business needs + Strong knowledge of medical conditions and how they apply to disability products + Professional oral, written and presentation skills + Strong PC skills, including Microsoft Office applications (MS Word, Excel, PowerPoint) + Knowledge of disability products, business rules and procedures, preferred + Experience with DCMS, Claim Facts, and iProcess preferred **You will** + Review short-term and or long-term disability claims to assess the impact of claimants' medical condition on their function as well as the impact of their medical treatment in achieving improved functional outcomes. + Possess excellent verbal and written communication skills to gather and report information accurately, ask appropriate questions to facilitate partnership with treating providers, claimants, and internal partners to encourage participation of claimant in appropriate treatment goals.
Clinical/Medical Editor II, Critical Care EBSCO Information ServicesClinical/Medical Editor II, Critical CareOlympia, WARemote$68,070–$97,240 / yearKeep library of current clinical content up to date and relevant + Take initiative to identify areas of potential product development + Make decisions in consultation with the Section Editor that affect larger groups and more junior team members + Serve as content specialist within specific content domain(s), facilitate topic enhancement and development, perform systematic literature surveillance, and regularly review content collection + Support culture of teamwork and writer development through effective editing and feedback + Maintain quality of content and participate in quality initiatives + Project co-manage/co-lead editorial tasks/initiatives as required with Section Editor or Editor-in-Chief + Other duties as assigned by supervisor **About You** + Bachelor's degree or higher in nursing + Nursing licensure current and in good standing + Direct patient care experience in critical care setting. Join the EBSCO talent community to receive updates on new opportunities that align with your skills and interests - register using the links below: Experienced Talent Community (https://talent.ebsco.com/exp/talentcommunity/form)
Principal Clinical Content- Physician - UpToDate, Physician Editor, Adult Neurology Wolters KluwerPrincipal Clinical Content- Physician - UpToDate, Physician Editor, Adult NeurologyOlympia, WA$173,500–$310,000 / yearQUALIFICATIONS** **Required Education:** - Medical Degree - Board Certification/Eligibility in Adult Neurology **Preferred Experience, Knowledge, and Abilities:** - Clinical experience in an academic setting after residency - A valid medical license in at least one U.S. state - Impeccable communication skills: verbal, writing, and listening - Ability to work collaboratively with colleagues at different skill levels - Self-motivated, with excellent organizational and time management skills - Ability to give and receive feedback effectively - Interest in critical analysis of the medical literature (skills can be learned on the job) - Ability to spend 80 to 90% of the work week on editorial work - Interest in and ability to maintain clinical work (10 to 20%) **TRAVEL** : Minimal - less than 5% \#LI-Hybrid **Our Interview Practices** _To maintain a fair and genuine hiring process, we kindly ask that all candidates participate in interviews without the assistance of AI tools or external prompts. Please note that use of AI-generated responses or third-party support during interviews will be grounds for disqualification from the recruitment process._ _Applicants may be required to appear onsite at a Wolters Kluwer office as part of the recruitment process._ **Compensation:** $173,500.00 - $310,000.00 USD This role is eligible for Bonus.
Clinical Nurse Manager American Oncology Network IncClinical Nurse ManagerOlympia, WA$73,486.40–$144,248 / yearAbility to build an engaging culture of quality, performance effectiveness and operational excellence through best practices, strong business and political acumen, collaboration and partnerships, as well as a positive employee, physician and community relations. Oversees the activities of the clinical areas and directs, organizes, and assigns work to the clinical team that includes nurses, medical assistants (if applicable), lab (if applicable) and pharmacy technician(s).