DCS CorporationOperations Research Analyst - Intermediate DCS CorporationOperations Research Analyst - IntermediateJoint Base Lewis-McChord, WAMA/MS/MBA from an accredited college or university in Operations research, management science, analytics, math, engineering, computer science, or another technical or quantitative field with 6 years in data analytics, 5 of which are in a supervisory or lead capacity. Under limited supervision, perform complex analytical analyses using advanced mathematical and analytical methods to help organizations investigate complex issues, identify and solve problems, and make better decisions.
CommonSpirit HealthNewGastroenterologist 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.
MultiCare Health SystemClinical 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.
MultiCare Health SystemClinical Research Coordinator Sr MultiCare Health SystemClinical Research Coordinator SrTacoma, WAFull timeIn addition to serving as lead coordinator on multiple clinical trials, the Senior Clinical Research Coordinator provides training, mentorship, project leadership, and quality control oversight of Coordinators and Research Assistants in assigned areas. Minimum 4 years of experience serving as lead coordinator conducting clinical trials required; worked as primary research coordinator for at least 10 drug or device trials.
MultiCare Health SystemClinical 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.
Providence St. Joseph HealthClinical 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.
MultiCare Health SystemResearch 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.
The Evergreen State CollegeResearch Associate The Evergreen State CollegeResearch AssociateOlympia, WAFull timeThe ideal candidate will have a background in policy analysis and a broad interest in evidence-based public policy; be a self-starter; be comfortable with ambiguity; possess strong quantitative, data analytical, communication, project management, and interpersonal skills; and have an eagerness to learn. A full state benefits package which includes: paid sick and vacation leave; paid campus holidays; a generous medical, dental, life and disability insurance package for employees and dependents; retirement; optional deferred compensation and optional supplemental retirement accounts.
The Henry M. Jackson FoundationClinical 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.
The Henry M. Jackson FoundationSenior Clinical Research Director (SCRD) The Henry M. Jackson FoundationSenior Clinical Research Director (SCRD)Tacoma, WA$120,600–$180,000 / yearFull timeTBICoE's mission to support the warfighter is executed through subject matter experts embedded across DHA facilities with expertise in TBI clinical research investigations, surveillance, clinical tool development and training, cognitive monitoring and assessment, and dissemination of TBI tools, products, and education/training materials to DoD medical personnel, service members, including Guard, Reserve, and operational medics/corpsmen, veterans with TBI, and families/caregivers of the warfighter. Ability to facilitate, present and translate information to diverse end users of research findings in small and large groups, inclusive of providers, scientists, line leaders, and other relevant TBI stakeholders, as well as the flexibility to re-prioritize quickly based on shifting gaps, taskers, leadership composition, and local/HQ requirements required.
The Henry M. Jackson FoundationResearch Scientist The Henry M. Jackson FoundationResearch ScientistTacoma, WA$88,600–$140,000 / yearFull timeTBICoE's mission to support the warfighter is executed through subject matter experts embedded across DHA facilities with expertise in TBI clinical research investigations, surveillance, clinical tool development and training, cognitive monitoring and assessment, and dissemination of TBI tools, products, and education/training materials to DoD medical personnel, service members, including Guard, Reserve, and operational medics/corpsmen, veterans with TBI, and families/caregivers of the warfighter. However, 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.
MultiCare Health SystemNewPhysician - Neurosurgeon MultiCare Health SystemPhysician - NeurosurgeonAuburn, WAFull timeThis role integrates operative expertise with high-acuity inpatient management and outpatient continuity, supporting a broad range of neurosurgical conditions including cranial, spinal, peripheral nerve, and functional disorders. Whether you're looking to advance your research, take on leadership opportunities, or be part of strategic initiatives that expand access to quality care, you'll find your place in our growing community of dedicated professionals.
ParexelSenior Clinical Research Associate/Clinical Research Associate II - Northeast, Southeast, Central U ParexelSenior Clinical Research Associate/Clinical Research Associate II - Northeast, Southeast, Central UOlympia, 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 SCP 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). 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.
ParexelClinical Research Associate/Senior Clinical Research Associate- FSP ParexelClinical Research Associate/Senior Clinical Research Associate- FSPOlympia, WAParexel FSP is looking for a CRA/Sr CRA in the MidWest and West region of the United States!** **Oncology Experience required.** **Job Purpose:** The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). + Follows 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.
ParexelSenior Clinical Research Associate/Clinical Research Associate II - FSP ParexelSenior Clinical Research Associate/Clinical Research Associate II - FSPOlympia, 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). 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.
HumanaSenior Clinical Policy Research Professional HumanaSenior Clinical Policy Research ProfessionalOlympia, WARemote$86,300–$118,700 / yearSuccess in this role requires:** + Strong organization skills and detail orientation + Excellent verbal and written communication skills + Strong analytical and web navigation skills + Self-direction with demonstrated ability to meet strict deadlines + Strategic thinking and planning capabilities **Use your skills to make an impact** **Required Qualifications** + Associate or bachelor's degree in dental hygiene or dental assisting + Appropriate state certification or licensure as a dental assistant or dental hygienist + 5 years or more of prior clinical experience + Proficiency with Microsoft Office products including Word and Excel **Preferred Qualifications** + Master's degree in health-or business-related field + Utilization management experience (Medicare or Medicaid) + Proven successful experience in compiling health-related research, with associated analysis and conclusions Travel: While this is a remote position, occasional travel to Humana's offices for training or meetings may be required. **Become a part of our caring community** The Senior Clinical Policy Research Professional works closely with Humana's dental directors and medical directors to research, develop and maintain dental and medical coverage policies utilizing an evidence-based medicine review process.
ParexelClinical 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.
ParexelSite and Monitoring Health Lead / Lead Clinical Research Associate - Northeast US - FSP ParexelSite and Monitoring Health Lead / Lead Clinical Research Associate - Northeast US - FSPOlympia, WAKey Accountabilities:** **Oversight of monitoring effectiveness** + Implements various types of oversight encounters and activities as applicable including but not limited to site risk analysis, site contacts, aggregate review of data, monitoring visit report review, Sponsor Oversight Visits, system/data spot checks, and periodic summaries; ensure timely documentation of these activities is completed and file + Completes Sponsor Oversite Visit reports consistently on time and with good quality + Utilizes a risk-based approach to review critical to quality items at the site level and study level, exhibiting an "inspection ready at all times" mentality + Creates Study Specific Oversight Plans (SSOPs) for aligned trials in scope and /or follows SSOP when conducting oversight activities + Troubleshoots and uses alternative and innovative approaches to solve problems impacting clinical site delivery and quality + Utilizes root cause analysis to assess identified issues and provide suggested actions to Study Management/Clinical Research Organization (CRO) to mitigate risk + Supports inspection preparation and management **Collaborative relationships** + Works both independently and collaboratively with cross-functional teams + Builds relationships with investigators and site staff in region; acts as a resource for identifying potential sites for new studies + Supports investigator sites less experienced in research; assists in assuring sites are engaged in the study and have what they need to recruit participants successfully + Works closely with Clinical Risk and Analytics staff to understand the risk management plan (Risk MAP) for assigned studies, ensures the SSOP is aligned with the Risk MAP, and assesses sites who are outliers **Operational** + Implements client Site and Monitoring Health strategy in alignment with applicable International Council for Harmonization-Good Clinical Practices (ICH-GCP) regulations + Leads oversight and trend meetings with the study team and/or Clinical Research Organization (CRO) to discuss risks, issues, and trends identified by the SMH team for the trial + Remains current with global regulatory requirements, has a current working knowledge of local/regional regulatory requirements **Skills:** + Ability to think innovatively and be willing to initiate changes, introduce new ideas, and creatively problem-solve + Ability to build and maintain relationships with key investigators and sites (e.g. **Job Purpose:** The Site and Monitoring Health Lead (SMH Lead) will apply knowledge of regulations and GCPs as well as experience in monitoring to safeguard the quality of clinical trial execution at investigator sites and ensure the client's oversight of CRO monitoring effectiveness.
ParexelSenior Clinical Research Associate - Oncology - Florida - FSP ParexelSenior Clinical Research Associate - Oncology - Florida - FSPOlympia, WAPerform drug accountability, reconciliation, and destruction, ensuring protocol compliance for storage and shipment requirements **Oversight Monitoring:** + Prepare and maintain Oversight Monitoring Plan + Perform review of study metrics, assess CRO Clinical Research Associate (CRA) and Investigator Site performance and identify sites for oversight monitoring visits + Conduct Oversight Monitoring Visits at sites, either independently or alongside CRO CRA + Review site source documentation and verify accurate data capture (ALCOA principles) + Review and report on status of study conduct at the investigator site ensuring appropriate follow up of any identified issues/action items **Documentation and Reporting:** + Ensure site regulatory files are current and verify timely submission of study documentation, including safety reporting. **Inspection Readiness** + Support inspection readiness activities and ensure sites maintain data integrity and protocol deliverables **JOB REQUIREMENTS:** **Education:** Bachelor's degree (or equivalent) **Experience:** + Minimum of 5 years of direct onsite monitoring/CRA experience in a CRO or pharma organization + Phase I Oncology monitoring experience required + Strong analytical problem-solving skills and critical thinking abilities.
ParexelNewSenior Clinical Research Associate - Midwest/Central US - FSP ParexelSenior Clinical Research Associate - Midwest/Central US - FSPOlympia, 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). 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.
Metis FoundationClinical 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.
Pharming HealthcareNewSenior Medical Director - Clinical Research Pharming HealthcareSenior Medical Director - Clinical ResearchOlympia, WARemote$310,000–$375,000 / yearParticipate in strategic planning as part of Medical Affairs, Marketing and Business Development teams + Provide medical and scientific leadership and support at key scientific meetings (US and International) + Extensive interactions with academic thought leaders to optimize and develop clinical trial strategies + Perform other duties as assigned **Qualifications** + Medical license in good standing in a U.S. State or Territory preferred + 5+ years in clinical development including managing CROs + Experience in product launch, regulatory filings and FDA communications highly preferred + Strong leadership and management skills + Strong verbal and written communication skills are essential + Exceptional interpersonal skills and problem-solving capabilities + Ability to work effectively across a global matrixed organization + Travel - Include 20% travel time required for the position where travel occurs locally or internationally, if applicable + Commitment and alignment to Pharming's mission, core values and behaviors **Salary Range** Pharming takes into consideration a combination of candidate's work experience, training, and education, as well as the scope of the role, complexity, and external market and internal value when determining a salary level. **Responsibilities** + Lead/support clinical development (strategy, develop protocols, study start-up, close-out, oversight, and regulatory support) for napazimone studies + Dedicated medical and scientific role to execute of the clinical strategy for the napazimone program, including + Support the pivotal napazimone studies for mtDNA Primary Mitochondrial Disease + Lead the napazimone pediatric study plan and clinical pharmacology studies + Lead the napazimone program for new indications + Work cross-functionally to define, plan, and implement studies + Lead the sponsor oversight of medical monitoring across the napazimone programs + Analyze and oversee data from clinical trials and produce reports, including safety data, efficacy data, completeness and trend analysis eCRF data, and oversight of protocol deviations + Lead clinical study site engagement in the US + Participating and providing clinical input into safety and regulatory interactions.
Bausch + LombNewResearch 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.
Sumitomo PharmaNewSenior Medical Director, Clinical Research (Ophthalmology) Sumitomo PharmaSenior Medical Director, Clinical Research (Ophthalmology)Olympia, WA$284,320–$355,400 / yearJob Duties and Responsibilities** + Responsible for and lead all activities related to clinical study design from clinical study concept to clinical study protocol for both early- and late-stage programs + Leads or joins multi-disciplinary, multi-regional, matrix team through highly complex decisions + Leads and drives strategy for clinical studies for assigned asset(s) within the Ophthalmology therapeutic area + Provides oversight of clinical trial conduct, interacting with CROs, medical monitors, and vendors as required, and working with the safety group to ensure adequacy of safety monitoring and reporting + Provide clinical input for and participate in study set up and design including data collection tools, data analysis, eCRF design, edit checks, vendor database design plans, etc. (https://c212.net/c/link/?t=0&l=en&o=4190475-1&h=3440496098&u=https%3A%2F%2Fwww.us.sumitomo-pharma.com%2F&a=https%3A%2F%2Fwww.us.sumitomo-pharma.com+) or follow us on LinkedIn (https://c212.net/c/link/?t=0&l=en&o=4190475-1&h=2504638834&u=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fsumitomo-pharma-america%2F&a=LinkedIn) .
Bausch + LombResearch 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.
Pacific Northwest National LaboratoryPost Doctorate Research Associate- Hardware-Software Co-design for Scalable AI Systems Pacific Northwest National LaboratoryPost Doctorate Research Associate- Hardware-Software Co-design for Scalable AI SystemsOlympia, WARockstar Rewards** Employees and their families are offered medical insurance, dental insurance, vision insurance, robust telehealth care options, several mental health benefits, free wellness coaching, health savings account, flexible spending accounts, basic life insurance, disability insurance*, employee assistance program, business travel insurance, tuition assistance, relocation, backup childcare, legal benefits, supplemental parental bonding leave, surrogacy and adoption assistance, and fertility support. **Security, Credentialing, and Eligibility Requirements** As a national laboratory, PNNL is responsible for adhering to the Homeland Security Presidential Directive 12 (HSPD-12) and Department of Energy (DOE) Order 473.1A, which require new employees to obtain and maintain a HSPD-12 Personal Identify Verification (PIV) Credential.
Sumitomo PharmaSenior 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_
CytelResearch 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.
University of WashingtonResearch Scientist (Temporary), RGUD University of WashingtonResearch Scientist (Temporary), RGUDOlympia, WAThe Reproductive, Genitourinary and Digestive (RGUD) disease estimation team maintains and advances quantitative understanding of the health impacts, levels and trends of digestive diseases (including liver conditions - cirrhosis, hepatitis, and non-alcoholic fatty liver disease), gynecological and urinary disorders, sexually transmitted infections, and maternal disorders, and a subset of endocrine, metabolic, blood and immune disorders. **Job Description** **The Institute for Health Metrics and Evaluation (IHME) has an outstanding opportunity for a Research Scientist to join their Reproductive, Genitourinary and Digestive (RGUD) disease estimation team.** **About this Opportunity** Reporting to the Acting Assistant Professor, the Research Scientist is responsible for driving high-impact global health research at IHME, analyzing quantitative data across causes of death, epidemiology, and social determinants to produce key estimates that inform global health policy.
Sumitomo PharmaNewDirector, Clinical Research Sumitomo PharmaDirector, Clinical ResearchOlympia, WA$192,320–$240,400 / 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. Key responsibilities: + Ownership of the key elements in planning and implementation of a clinical development program or programs in support of the overall product development plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, and emerging issues.
GovCIOOperations Research Analyst / Data Scientist (Remote) GovCIOOperations Research Analyst / Data Scientist (Remote)Olympia, WARemote$90,000–$100,000 / yearWhat You Can Expect** **Interview & Hiring Process** If you are selected to move forward through the process, here's what you can expect: + During the Interview Process + Virtual video interview conducted via video with the hiring manager and/or team + Camera must be on + A valid photo ID must be presented during each interview + During the Hiring Process + Enhanced Biometrics ID verification screening + Background check, to include: + Criminal history (past 7 years) + Verification of your highest level of education + Verification of your employment history (past 7 years), based on information provided in your application **Employee Perks** At GovCIO, we consistently hear that meaningful work and a collaborative team environment are two of the top reasons our employees enjoy working here. + 5+ years of work experience (2 years of experience may be removed for a masters degree) + 2+ years of experience in data exploration, data cleaning, visualization, and overall data analytics + 2+ years of experience in data visualization tools such as Qlik or PowerBI **Preferred Skills and Experience:** + Experience in distributed data and computing tools including Databricks + Experience with data modeling, mapping data flows and data design.
OracleSenior Research Scientist- RWE/Harm Reduction OracleSenior Research Scientist- RWE/Harm ReductionOlympia, WA$79,100–$158,200 / yearResearch Scientist in RWE Tobacco Harm Reduction, you will: + Be the Principal Investigator, lead the design of behavioral studies (e.g., Actual Use, PMSS, TPPI) including writing research proposals, collaborating on protocol and statistical analysis plan (SAP) development, overseeing data analysis, providing analytical interpretation, writing reports, abstracts, posters, and manuscripts. To succeed, you will need: + Minimum a MPH or Master's with 5+ years of industry experience or PhD with 5 years of independent research experience - any advanced degree in epidemiology, public health, or related discipline + Must have experience in survey design and quantitative methods + Strong scientific writing and presentation skills for client engagement.
Capital OneSenior Manager, Data Science - Quantum Computing Research (Remote-Eligible) Capital OneSenior Manager, Data Science - Quantum Computing Research (Remote-Eligible)Olympia, WARemote$209,000–$238,500 / yearBasic Qualifications:** + Currently has, or is in the process of obtaining one of the following with an expectation that the required degree will be obtained on or before the scheduled start date: + A Bachelor's Degree in a quantitative field (Statistics, Economics, Operations Research, Analytics, Mathematics, Computer Science, or a related quantitative field) plus 7 years of experience performing data analytics + A Master's Degree in a quantitative field (Statistics, Economics, Operations Research, Analytics, Mathematics, Computer Science, or a related quantitative field) or an MBA with a quantitative concentration plus 5 years of experience performing data analytics + A PhD in a quantitative field (Statistics, Economics, Operations Research, Analytics, Mathematics, Computer Science, or a related quantitative field) plus 2 years of experience performing data analytics + At least 2 years of experience leveraging open source programming languages for large scale data analysis + At least 2 years of experience working with machine learning + At least 2 years of experience utilizing relational databases **Preferred Qualifications:** + Ph. Remote (Regardless of Location): $209,000 - $238,500 for Sr Mgr, Data Science McLean, VA: $229,900 - $262,400 for Sr Mgr, Data Science Candidates hired to work in other locations will be subject to the pay range associated with that location, and the actual annualized salary amount offered to any candidate at the time of hire will be reflected solely in the candidate's offer letter.
EYNewBusiness Tax Services - Federal Tax Advisory - Research & Credits Senior Manager EDGE EYBusiness Tax Services - Federal Tax Advisory - Research & Credits Senior Manager EDGEOlympia, WA$130,600–$298,700 / yearof the QS/R&D offshore (GDS team) in multiple global locations, including development of optimal collaboration model with US Edge STEM R&D team + Play critical role with the identification, development and introduction of new/improved tools/technologies to increase quality and efficiency of R&D engagement execution + Advise on determining the optimal mix/structure of specialty support teams (Edge STEM, GDS, Edge data, etc.) and individual resources in order to achieve optimal quality, efficiency, margin, etc., for each significant research credit engagement + Using specific scientific, engineering and/or computer science expertise, analyze and interpret detailed technical engineering/software development documentation to assist in making determinations as to whether certain activities meet the requirements for research credits/incentives + Provide technical feedback on specific technical deliverables prepared by the Edge STEM and GDS team members on specific client engagements as well as overall quality assurance/review for both teams more broadly + Interpret case law to apply the facts and circumstances effectively to client facts + Directly supervises all aspects and all members (Staff - Manager) of the US QS Edge R&D team, as well as indirectly supervises the execution and work product quality produced by the GDS R&D team members + Must be able to effectively work on multiple projects (leadership/practice management as well as client engagements) simultaneously + Able to prioritize or request clarification on the priority of various engagements + Responsible for management of daily project tasks in order to meet client deadlines + Provide regular status updates to and communicate daily with NTD QS/Edge leadership team **Skills and attributes for success** **To qualify for the role you must have** + A bachelor's degree in a related field (i.e. engineering, science, computer programming, etc.) or equivalent experience + Minimum of 8-10 years professional research credit firm experience + Detailed knowledge of the rules and tax technical qualification requirements for the US Federal research tax credit as well as potentially other US and foreign R&D incentives + Basic knowledge of the use and navigation of Prodigy + Ability to manage multiple projects simultaneously + Responsible for management of own daily project tasks in order to meeting client deadlines + Ability to collaborate effectively + Strong organizational and verbal communication skills + Flexibility with client demands and tight deadlines + Ability to work overtime when needed to meet client needs + Willingness to travel - some travel, whether for client/engagement or internal meetings, is required **Ideally you also have** + Microsoft certifications or experience in the below applications: 1. **Your key responsibilities** + Oversee all aspects of the US Edge R&D STEM team, including: + General administration/management of the team + Day-to-day operations + Recruiting + Onboarding + Development and implementation of training (process, tax technical, technology, etc.) + Staffing/client assignments/team utilization + Quality review process + Process & workflow development/improvement, best practices + Customer satisfaction of R&D engagement teams + Lead detailed technical interviews for select R&D engagements/pursuits with client engineers, scientists and software developers to determine eligibility/qualification for R&D tax credits and incentives + Utilize specific STEM expertise to make and assist other team members with technical determinations as to whether certain activities meet the requirements for research credits/incentives based on the results of technical interviews and surveys/questionnaires prepared by client STEM personnel + Review various tax- and STEM-technical memos and other technology/engineering discipline-specific client deliverable documents (e.g.
MerckSenior Director, Clinical Development - Antibacterials, Antifungals, CMV & Covid 19 MerckSenior Director, Clinical Development - Antibacterials, Antifungals, CMV & Covid 19Olympia, WA$282,200–$444,200 / yearRole may be remote **Specifically, the Senior Director may be responsible for:** · Planning clinical trials (design, operational plans) based on the clinical development strategies for investigational or marketed infectious disease drugs · Monitoring and managing the conduct of ongoing or new clinical trials for investigational or marketed infectious disease drugs · Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publications · Participation in internal and joint internal/external research project teams relevant to the development of investigational drugs, and the further study of marketed drugs · Developing clinical development strategies for investigational or marketed infectious disease drugs · Presenting study data and program strategic plans to internal governance committees for endorsement and key program milestones **The Senior Director is responsible for maintaining a strong scientific fund of knowledge by:** · Maintaining awareness of scientific developments within their area of expertise, including new scientific findings and research methodologies · Establishing communications with prominent clinical investigators in their particular field of interest, particularly those scientifically and operationally strong investigators who can assist in the development of our company's investigational and marketed drugs · Attending appropriate scientific meetings to maintain their competency and to maintain awareness of research activities in their area of responsibility. **To accomplish these goals, the Senior Director may:** · Author detailed development documents and presentations for internal and external audiences · Author scientific publications · Facilitate collaborations with external researchers around the world · Travel on company business up to about 10% of the time to manage future or ongoing clinical research projects.
IQVIASpanish 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.
United TherapeuticsMonitoring Team Lead / Senior Monitoring Team Lead United TherapeuticsMonitoring Team Lead / Senior Monitoring Team LeadOlympia, WA$105,500–$140,000 / yearThey will be functionally responsible for study assigned Clinical Monitoring team members (central, field, contract and permanent staff), monitoring activities, and support of study sites to ensure compliance with United Therapeutics Corporation (UTC) process, applicable regulations and industry guidance throughout the duration of the trial. The cure for end-stage life-threatening diseases like PAH, PH-ILD, PF, and many others is an organ transplant, but only a small percentage of donated organs are available to address the vast need.
Cardinal HealthClinical Manager, Gastroenterology (GI) Customer Success Cardinal HealthClinical Manager, Gastroenterology (GI) Customer SuccessOlympia, WARemote$105,100–$150,000 / yearManage the details and overall workflow for the Clinical Analyst to onboard new practices including Assessment Call and giving direction to Clinical Analyst owning account + Manage the training and oversite of all new Clinical Analyst Team members (working with HR, technology teams, onboarding checklist, etc.) + Manage the ongoing skills assessments and competency testing of all Clinical Analyst Team Members + Manage the build of any new disease states, needed educational materials, etc. for defined workflows and "play books" per GI disease states + Manage the customer/practice experience regarding value of PPS services, impactful and accurate reporting and consistent messaging through presentations, slide decks, emails etc. **_Qualifications_** + Individuals with a strong GI background: BSN and RN license highly preferred, APP licensure a plus + 5+ years of clinical experience preferred + Ideally targeting 5-8 years of experience working in a GI Office Practice (2 years of experience in a supervisory or management role in a GI Office Practice) preferred + Must bring an analytical mindset with the willingness/ability to take a data-driven approach + Strong communication skills are necessary in this role as this individual will be leading presentations for various stakeholders + Knowledge of medical terminology required + Knowledge of health-care related computer applications including practice management systems, electronic health record systems, etc.
Otsuka America Pharmaceutical Inc.NewDirector, Global Clinical Development Otsuka America Pharmaceutical Inc.Director, Global Clinical DevelopmentOlympia, WAResponsibilities** : Otsuka is seeking an Associate Director/Director/Senior Director, Global Clinical Development based in our Rockville, MD or Princeton, NJ offices, who will be responsible for the design and oversight of clinical research programs and protocols for OPDC products under good clinical practices (GCP). + Its goal is to efficiently evaluate the product's potential and probability of success, support an effective commercial launch and plan for meaningful innovations to improve or expand the value of the initial product for our global customers (patients, prescribers and payors).
Canon USA & AffiliatesLeader Medical Affairs Canon USA & AffiliatesLeader Medical AffairsOlympia, WA10 years' experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting or 3 years of experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting plus 7 years of experience in healthcare industry as imaging scientist or research manager. **Leader Medical Affairs - req1704** **OVERVIEW** Lead a team of clinical and technical experts dedicated to positively impacting clinical care by effectively translating innovative imaging solutions to the clinical environment.
MerckClinical Quality Operations Manager, Oncology MerckClinical Quality Operations Manager, OncologyOlympia, WA$142,400–$224,100 / yearInspection Preparation and Management:** The CQOM is responsible for maintaining current regulatory inspection knowledge as it relates to Good Clinical Practice (GCP) inspections by regulatory agencies worldwide, especially those conducted by key authorities such as the USA Food and Drug Administration, European Medicines Agency, UK Medicines and Healthcare products Regulatory Agency, as well as other established and emerging authorities. + Develops the strategy for management/support for GCP inspections of Company products to ensure that all phases of Regulatory Health Authority inspections (i.e. inspection preparation, management and follow up) are handled consistently, professionally and proactively and result in outcomes that demonstrate the Company's dedication to regulatory compliance.
ParexelSite Care Partner - Central/Midwest or West Coast - FSP ParexelSite Care Partner - Central/Midwest or West Coast - FSPOlympia, WAThis role also contributes to site selection, provides local intelligence, ensures site support, resolves issues, and collaborates with various functions to optimize communication, maintain site quality and patient safety utilizing data analytics to identify and mitigate risks. The Site Care Partner is a crucial liaison for investigative sites throughout a study's lifecycle, responsible for site start-up, activation, relationship management, recruitment, and quality assurance.
ParexelBiotech Project Leadership - Clinical Trials - Home- Based - (Future Needs) ParexelBiotech Project Leadership - Clinical Trials - 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 future 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 Neurology, Oncology (Hematology), Respiratory, Cardio, General Medicine and GLP-1 /Obesity.**
IQVIANewField Nurse Educator - Tacoma, WA IQVIAField Nurse Educator - Tacoma, WATacoma, WA$95,000–$105,000 / yearAbility to support multiple disease states and medications as needed · Provide patient-focused education to promote behavioral change for the empowerment of patients to improve specific treatment compliance · Foster appropriate dialogue between patient and health care provider Job Qualifications: · Bachelor's degree and/or BSN preferred · RN licensure required in state of residency - compact multi-state license as available per state · Current nursing license in good standing · 5 + yrs. Nurse Educators provide education about specific disease treatments, and resources to help patients better begin and manage their disease state and resources associated with their prescribed medication.
ParexelNewProject Specialist - (Clinical Trials) - Home-Based ParexelProject Specialist - (Clinical Trials) - Home-BasedOlympia, WARemoteThe Project Specialist is the liaison and communication hub to all the global functional teams working on a project, ensuring all team members are updated and on the same page during the entire project life cycle, contributing to achievement of study deliverables. Collect information from FLs and team members in order to prepare study templates, documentation, customization of forms and spreadsheets for study, adding version control and filing in TFM system.
Virginia Mason Franciscan HealthGastroenterologist Hospitalist Physician Virginia Mason Franciscan HealthGastroenterologist Hospitalist PhysicianTacoma, 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. Our comprehensive network of 10 hospitals and nearly 300 care sites strategically located across the greater Puget Sound region reflects our ongoing commitment to accessibility and comprehensive care.
OracleNewSenior Principal Software Developer OracleSenior Principal Software DeveloperOlympia, WA$96,800–$251,600 / yearWith your superb technical, research and analytical capabilities and demonstrated ability to get the right things done quickly and effectively to delight our customers, you will envision, collaborate with executives for investment and drive the software design and development for new major data-plane components of Oracle's Cloud Infrastructure. + A journaling service that reliably and efficiently records sequential, immutable logs (journal entries) of operations or transactions, with architecture designed to support increases in workload (scalability), while consistently delivering very fast response times for both recording and retrieving journal entries (low latency).
OracleOncology 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.
ParexelNewClinical Laboratory Study Manager - FSP ParexelClinical Laboratory Study Manager - FSPOlympia, WAWorks with Precision Medicine Strategy Lead as well as clinical study teams, data management (DM) team, Samples, Kits, Data, Logistics (SKDL) and Clinical Laboratory Project Management (CLPM) groups to ensure quality samples and data are delivered to support biomarker and non-biomarker evaluation and enable the translation of science to medicine. Will work closely with project managers (central and/or specialty labs) and lend expertise to clinical trial management (CTM) and CRO to ensure samples are collected per protocol and assist with resolving any sample related issues or queries.
Wolters KluwerPrincipal 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.