220 Results for

Research Jobs in Parkland, WA

Jobs

Joint Base Lewis-McChord, Washington12 days ago

MA/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.

Lakewood, WA14 days ago

Our 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.

Tacoma, WA30+ days ago

Full-time
Employee

This 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.

Tacoma, WA30+ days ago

Full-time
Employee

In 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.

Tacoma, WA30+ days ago

Part-time
Employee

Minimum 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.

Lacey, WA30+ days ago

Part-time
Employee

Our 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.

Tacoma, WA30+ days ago

$25–$28 Per Hour
Temporary
Contractor
Part-time

Responsible for working with research team and coordinating travel arrangements within University and military systems to include managing booking of airfare, hotel, and rental cars and assisting team with any paperwork needed for other costs. Responsible for learning the ordering process, ordering supplies, monitoring supplies to ensure all supplies ordered do not expire prior to data collection, and track purchases within University level systems and for grant agency reporting.

Tacoma, WA15 days ago

Full-time
Employee

Home 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.

Olympia, WA30+ days ago

Full-time
Employee

The 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.

Tacoma, WA30+ days ago

Full-time
Employee

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. 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.

Lacey, WA30+ days ago

Part-time
Employee

Our 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. Our award-winning and comprehensive medical centers are known for outstanding programs in cancer, cardiology, neurosciences, orthopedics, women's services, emergency and trauma care, pediatrics and neonatal intensive care.

New!

Renton, WA2 days ago

Full-time
Employee

The Medical Policy Research Analyst Intern will primarily identify, appraise, and summarize scientific literature and clinical practice guidelines for the development and implementation of medical policies to be used by Medical Directors, internal clinical staff, and external providers and members. * Knowledge of techniques for conducting literature searches, analyzing and interpreting scientific medical literature for quality of study design and reliability of data.

Tacoma, WA30+ days ago

$120,600–$180,000 Per Year
Full-time
Employee

TBICoE'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.

Tacoma, WA30+ days ago

$88,600–$140,000 Per Year
Full-time
Employee

TBICoE'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.

Renton, WA15 days ago

Full-time
Employee

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. Planning, organizing, developing, directing, coordinating and evaluating the human and material resources necessary to support completion of research studies led or co-led by registered nurses, with interprofessional teams.

Newcastle, WA26 days ago

$66,000–$76,000 Per Year
Full-time
Employee

Other compensation includes discretionary bonus; 9 paid holidays per year; PTO/sick leave 1 hour per 25 hours worked (max 160 hours). Investment/Market Research Analyst sought by Prime Metropolis Properties, Inc., position based in Newcastle, Washington.

Renton, WA30+ days ago

Remote

Full-time
Employee

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. This role focuses on preventing and reducing unnecessary spending by scoping PI initiatives, analyzing claims data, developing a thorough implementation assessment plan, and collaborating with internal and external stakeholders to optimize the payment processes.

Renton, WA16 days ago

Remote

Full-time
Employee

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. This role focuses on preventing and reducing unnecessary spending by scoping PI initiatives, analyzing claims data, developing a thorough implementation assessment plan, and collaborating with internal and external stakeholders to optimize the payment processes.

Tumwater, WA30 days ago

Full-time
Employee

You will work closely with development partners and key stakeholders to iteratively design, develop, and deliver products and surfaces that will delight our customers. At Cribl, we partner with IT and Security teams at many of the world's biggest enterprises, including half of the Fortune 100, to bridge the gap between AI ambition and infrastructure reality.

New!

Seattle, WA1 day ago

You bring: - Consultative skills - the ability to listen, understand customer needs, and translate them into technical solutions - Technical leadership - comfort guiding architectural design decisions and deep-diving into implementation details - Intellectual curiosity - a drive to keep your technical skills current while maintaining a pulse on industry trends - Communication skills - experience presenting to small and large groups, from whiteboard sessions to executive briefings - Operational awareness - understanding of web site/services operations, management, and security Key job responsibilities - Own the technical engagement and success of customer implementation projects - Design cloud architectures leveraging AWS services - Provide thought leadership on security best practices for applications, servers, and networks - Respond to RFPs and define implementation approaches - Serve as a subject matter expert on security as it relates to customer applications and services - Lead whiteboard sessions, technical deep-dives, and presentations for audiences of all sizes - Capture and share best practices across the SA community - Collaborate with and learn from some of the brightest technical minds in enterprise architecture - Mentor peers and customers while staying current on AWS innovations and industry trends - Travel up to 30% A day in the life You'll provide architectural and technical leadership to nonprofit customers leveraging AWS at scale. USA, CA, San Diego - 131,300.00 - 177,600.00 USD annually USA, NY, New York - 144,500.00 - 195,400.00 USD annually USA, VA, Arlington - 131,300.00 - 177,600.00 USD annually USA, WA, Seattle - 131,300.00 - 177,600.00 USD annually

Renton, WA30+ days ago

Full-time
Employee

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. The SPO reviews proposals, negotiates and administers federal and non-federal grants and contracts as well as evaluating organizational compliance with agreement terms, and assisting in the development of organizational processes and polices to ensure they meet established sponsor requirements.

Tacoma, WA30+ days ago

Full-time
Employee

This 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.

Olympia, WA30+ days ago

Work 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.

New!

Olympia, WA5 days ago

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. 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.

Olympia, WA30+ days ago

Work 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.

Seattle, WA11 days ago

Obtain, abstract, and code clinical information from multiple sources (medical records, research records, etc) for research participants in order to enter data into study specific data capture systems, and to document, assess, and report adverse events and safety data to study investigators, sponsors, IRB's and other regulatory authorities when applicable. \#UWDeptMedicineJobs **Compensation, Benefits and Position Details** **Pay Range Minimum:** $65,352.00 annual **Pay Range Maximum:** $84,996.00 annual **Other Compensation:** - **Benefits:** For information about benefits for this position, visit https://www.washington.edu/jobs/benefits-for-uw-staff/ **Shift:** First Shift (United States of America) **Temporary or Regular?**

Seattle, WA7 days ago

UWDeptMedicineJobs **Compensation, Benefits and Position Details** **Pay Range Minimum:** $78,600.00 annual **Pay Range Maximum:** $130,668.00 annual **Other Compensation:** - **Benefits:** For information about benefits for this position, visit https://www.washington.edu/jobs/benefits-for-uw-staff/ **Shift:** First Shift (United States of America) **Temporary or Regular?** **_About this Opportunity_** Reporting to the Research Manager, the Research Coordinator will take a lead role in conducting and managing a clinical research program undertaking studies that focus on the adult cystic fibrosis patient population.

Olympia, WA11 days ago

Remote

$86,300–$118,700 Per Year

Success 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.

Olympia, WA14 days ago

Work 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.

New!

Olympia, WA2 days ago

Work 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.

Olympia, WA8 days ago

Perform 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 related experience for Senior CRA + Strong analytical problem-solving skills and critical thinking abilities.

Joint Base Lewis-McChord, WA28 days ago

$60,000–$70,000

The 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.

Seattle, WA13 days ago

Obtain, abstract, and code clinical information from multiple sources (medical records, research records, etc) for research participants in order to enter data into study specific data capture systems, and to document, assess, and report adverse events and safety data to study investigators, sponsors, IRB's and other regulatory authorities when applicable. \#UWDeptMedicineJobs **Compensation, Benefits and Position Details** **Pay Range Minimum:** $57,600.00 annual **Pay Range Maximum:** $75,000.00 annual **Other Compensation:** - **Benefits:** For information about benefits for this position, visit https://www.washington.edu/jobs/benefits-for-uw-staff/ **Shift:** First Shift (United States of America) **Temporary or Regular?**

New!

Olympia, WA2 days ago

Remote

$310,000–$375,000 Per Year

Participate 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.

New!

Seattle, WA2 days ago

$97,665–$146,497 Per Year

Together, 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. #HOPECARECURE** Our founding promise to the community is as valid today as it was over a century ago: we will care for all children in our region, regardless of the families' ability to pay.

Seattle, WA13 days ago

The Clinical Research Billing Specialist will: + Support Billing team through day-to-day problem-solving in collaboration with or in the absence of Clinical Research Billing Manager and Lead; + Maintain a partial portfolio of research billing review, while managing unit work assignments and performing quality control review; + Be a day-to-day resource to the Billing team; and + Identify inconsistencies across the work product created by team members and recommend solutions in collaboration with colleagues and the unit's Manager and Lead **DUTIES AND RESPONSIBILITIES** **Epic Research Billing Workflows (30%)** + Research Billing Review: + Ensure charges route according to study billing grid, and in accordance with Epic charge documentation + Prioritize high-dollar and aging accounts + Charge Review and Claim Edit: Ensure research charges/claims have required coding for billing + No Rules and other escalations: Handle research billing questions escalated from Research Billing Coordinators and other departments **Epic Single Business Office (SBO) Research Invoicing Workflows (30%)** + Ensure timely generation of SBO invoices + Receive and process invoice corrections, including claims of "missing" charges + Process invoice payments + Follow up on aging research invoices to ensure payment **OnCore Clinical Trials Management System (CTMS)/Epic Interface (20%)** + Ensure accurate handoff from OnCore to Epic when study is activated or amended + Ensure accurate handoff from OnCore to Epic when subject enrollment updated + Perform Quality Control (QC) of study and enrollment records, providing feedback to study teams as needed **Patient Claims Review (10%)** + Respond to questions regarding patients' research study participation and the relationship to patient billing + Escalate issues to Team Lead or Manager as appropriate **Medicare Rules: Application and Training (10%)** + Understand and exercise independent judgment and discretion in the interpretation and application of the Medicare National Coverage Determination for Routine Costs in Clinical Trials, and all relevant UW Medicine clinical research budgeting and billing policies and procedures + As needed, provide training and education to Clinical Research Budget & Billing (CRBB) colleagues, School of Medicine investigators, research staff and practice site staff on research billing policies, procedures and tools + Provide excellent customer service and accurate guidance to clinical research study teams regarding clinical research billing policies and procedures + Assist in development of content for CRBB website and outreach documents + Assist faculty, staff and others in interpreting internal and external research billing policies **MINIMUM REQUIREMENTS** + A Bachelor's degree in science, business, healthcare administration or related field and at least two years related experience or equivalent combination of experience and education. **POSITION PURPOSE** The Clinical Research Billing Specialist position will enable the Clinical Research Billing Manager and Lead to coordinate and engage in the planning and implementation of new processes and systems without negatively impacting day-to-day unit management, responsiveness to customer concerns, proper training of new and existing members of the team and quality control of the unit's output.

Seattle, WA8 days ago

$29.16–$43.73 Per Hour

Our Principal Investigators (PIs) conduct studies in partnership with two multicenter research networks: the CDC-sponsored New Vaccine Surveillance Network and the HRSA-sponsored Pediatric Emergency Care Applied Research Network (PECARN). Together, 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.

Seattle, WA19 days ago

$152,360–$184,628 Per Year

Work-life benefits include:** Paid Time Off + US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees) + Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. + **Exceptional scientific communication and writing skills** , with demonstrated track record in manuscript writing and proven ability to collaborate effectively across cross-functional teams in a fast-paced, highly matrixed environment while managing completing priorities and tight timelines.

New!

Seattle, WA2 days ago

$73,378–$110,066 Per Year

Together, 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. This position will also assist with research related procedures and clinical activities as outlines and permitted within the Medical Assistant - Registered scope of practice as defined by Washington State Department of Health and Seattle Children's policy.

New!

Seattle, WA2 days ago

$35.28–$52.92 Per Hour

Together, 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. This position will also assist with research related procedures and clinical activities as outlines and permitted within the Medical Assistant - Registered scope of practice as defined by Washington State Department of Health and Seattle Children's policy.

Seattle, WA30+ days ago

$136,000–$184,000 Per Year

Basic Qualifications Position Requirements: PhD or foreign equivalent degree in Statistics, Psychometrics, Educational Measurement, Quantitative Psychology, Data Science, Industrial-Organizational (I/O) Psychology, or a related field and one year of research or work experience in the job offered, or as a Research Scientist, Research Assistant, Software Engineer, or a related occupation. Position Requirements: PhD or foreign equivalent degree in Statistics, Psychometrics, Educational Measurement, Quantitative Psychology, Data Science, Industrial-Organizational (I/O) Psychology, or a related field and one year of research or work experience in the job offered, or as a Research Scientist, Research Assistant, Software Engineer, or a related occupation.

Seattle, WA7 days ago

$152,360–$184,628 Per Year

Position Responsibilities** In the role as a Principal Scientist within the Cell Therapy Translational Research team, the ideal candidate: + Develop and implement end-to-end translational research strategies for cell therapy clinical trials + Partner with biostatisticians and computational biologists to provide timely analysis and communication of data and present its context and impact + Develop concepts and mechanism of action hypotheses identifying distinguishing characteristics of BMS cell therapy products alone or in combination with other therapies + Maintain a deep understanding of biomarker assays including flow cytometry, transcriptomics, proteomics and the application and use of these technologies in the clinical trial setting + Independently manage internal projects in cell therapy drug development + Serve on internal cross functional project teams and committees as scientific functional lead + Oversight and management of CROs and academic collaborators + Communicate regularly and prepare and make presentations within the department, externally, and to internal governance committees as required. **Work-life benefits include:** Paid Time Off + US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees) + Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.

Seattle, WA7 days ago

About this Opportunity** Reporting to the Interventional Trials Manager, the Research Coordinator will support multiple translational and clinical research studies focused on lung infection, inflammation, and immunity in the Translational and Interventional Trials Research Group at Harborview Medical Center within the University of Washington's Division of Pulmonary, Critical Care, and Sleep Medicine **Key Responsibilities** Research Subject Screening for Eligibility and Enrollment - 50% · Screening of University of Washington Medical Center patients through the electronic medical record (EMR) on Epic · Assessment of research study eligibility per protocol's inclusion/exclusion criteria · Obtainment of informed consent with research subjects or their legal next of kin · Coordination of biological sample collection (e.g. respiratory samples, blood, urine) · Close interaction with clinical providers to ensure patient safety and protocol adherence · Leading the establishment of improved screening workflows in collaboration with study teams and clinical staff · Managing study regulatory compliance, including compliance with all aspects of Institution and sponsor regulations pertaining to clinical research in human subjects Specimen Processing and Management - 30% · Leading processing of human biospecimens (e.g.

Seattle, WA16 days ago

Preferred Qualifications** + At least one year of full-time laboratory experience + Proficient in modern peptide synthesis, purification and analysis + Familiarity with peptide chemistry or synthetic chemistry or medicinal chemistry + Experience with lab instrument use and upkeep of: peptide synthesizers (CEM, Gyros), LC/MS (Agilent), HPLC systems (Agilent). Peptide Core is seeking a RSE Assistant to join a Core focused on producing synthetic peptides to continuously support many projects in parallel at the IPD, such as biologic therapeutics, phosphopeptide synthesis and characterization, difunctional fluorescent peptides, and peptide materials.

Seattle, WA11 days ago

This position will, under general direction from the principal investigator, perform professional-level support requiring scientific knowledge and skills regarding research involving human subjects for the grant titled "A Pilot Randomized Controlled Trial to Support Parent-Child Relationships Among Families with Elementary School-Aged Children Referred to Child Welfare," funded by the SON Research and Intramural Funding Program. - Experience as a current or previous Washington State Children's Administration/Department of Children, Youth, & Families (DCYF) and/or Department of Social and Health Services (DSHS) vetted employee or volunteer as required by our Washington State Institutional Review Board (WSIRB) approved protocol, and knowledge of confidentiality within the DCYF environment.

Seattle, WA21 days ago

Additional Qualifications** + Proficient in using Microsoft Office **Preferred Qualifications** + Knowledge of medical terminology + Knowledge of Epic + Experience in an inpatient setting with trauma patients + BA Degree in relevant field **Working Conditions** + This position is 100% on-site + The position's work is located at HMC + This position will work in an inpatient setting trauma patients + May need to work evening and night hours as required by study. + Communicate with the hospital personnel on possible procedures and treatments that will affect the subject's enrollment + Communicate with patients and/or family members to provide an explanation of the study and consent form + Communicate with lead Research Study Coordinator and/or Research Manager on subject enrollment.

Seattle, WA12 days ago

$89,300–$152,400 Per Year

Research Associate with a minimum of one year of experience: Des Moines, IA: $89,300 - $120,650 / year Denver/Chicago: $103,400 - $139,700 / year Seattle/New York City: $112,800 - $152,400 / year Research Associate with a minimum of three years experience: Des Moines, IA: $110,200 - $148,200 / year Denver/Chicago: $127,600 - $171,600 / year Seattle/New York City: $139,200 - $187,200 / year **Time Off Program** Flexible Time Off (FTO) is provided to salaried (exempt) employees and provides the opportunity to take time away from the office with pay for vacation, personal or short-term illness. **Who You Are** + Bachelor's degree + 1+ years equity research experience in the Healthcare sector (more than two is preferred) + High proficiency with financial statement analysis and fluent in overall financial accounting + Outstanding knowledge of financial modeling, quantitative financial analysis, statistics and accounting expertise + Possess the ability to synthesize data and articulate findings through exemplary presentation and communication skills (both written and verbal) + Entrepreneurial mindset; self-starter with a desire to earn option to build out individual coverage within our Healthcare dedicated team Travel as needed for conferences, management meetings, site visits, etc.

New!

Olympia, WA2 days ago

$284,320–$355,400 Per Year

Job 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) .

Seattle, WA16 days ago

$77,000–$214,000 Per Year

Specialty/Competency:** General Tax Consulting **Industry/Sector:** Not Applicable **Time Type:** Full time **Travel Requirements:** Up to 20% A career in our Specialised Tax Services practice, within Corporate Tax services, will provide you with the opportunity to help our clients meet their tax obligations while managing the impact tax has on their business. You are expected to focus on building client relationships, developing a deeper understanding of the business context, and navigating increasingly complex situations to grow your personal brand and technical knowledge.

Seattle, WA8 days ago

$51.65–$77.48 Per Hour

Together, 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. We offer specialized clinics dedicated to treating children with **cystic fibrosis** and **asthma** , and provide general evaluations for symptoms like coughing, shortness of breath, recurrent pneumonia, wheezing, chest pain, and exercise intolerance.

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