29 Results for

Winter Research Jobs in Olympia, WA

Jobs

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.

Olympia, WA30+ days ago

Full-time
Employee

The salary range (or starting rate for interns and associates) for this role represents numerous factors considered in the hiring decisions including, but not limited to, education, skills, work experience, certifications, location, etc. This includes individuals who will one dayrequest or require RSM to file or complete immigration-related forms or prepare letters on their behalf in order for them to obtain or continue their work authorization.

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.

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, WA19 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

$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

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.

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.

Olympia, WA9 days ago

Parexel 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.

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.

Olympia, WA18 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.

Olympia, WA22 days ago

Key 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.

Olympia, WA15 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, WA12 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 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.

New!

Olympia, WA6 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.

New!

Olympia, WA1 day ago

$130,600–$298,700 Per Year

of 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.

Joint Base Lewis-McChord, WA30+ 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.

New!

Olympia, WA6 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!

Olympia, WA6 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) .

New!

Olympia, WA6 days ago

$192,320–$240,400 Per Year

Sumitomo 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.

Olympia, WA28 days ago

$284,320–$355,400 Per Year

Sumitomo 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_

Olympia, WA21 days ago

$125,500–$230,200 Per Year

Distributed data technologies (e.g., Pyspark) + Cloud platform deployment and tools (e.g., Kubernetes) + Relational SQL databases + DevOps and continuous integration + GitHub + Strong organizational skills with the ability to manage multiple projects simultaneously and operate as a leading member across globally distributed teams to deliver high-quality services and solutions. If you have a disability and either need assistance applying online or need to request an accommodation during any part of the application process, please call 1-800-EY-HELP3, select Option 2 for candidate related inquiries, then select Option 1 for candidate queries and finally select Option 2 for candidates with an inquiry which will route you to EY's Talent Shared Services Team (TSS) or email the TSS at ssc.customersupport@ey.com .

Olympia, WA12 days ago

$105,500–$140,000 Per Year

They 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.

Tacoma, WA30+ days ago

Remote

Key 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.

Olympia, WA14 days ago

$282,200–$444,200 Per Year

Role 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.

Olympia, WA20 days ago

Remote

$105,100–$150,000 Per Year

Manage 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.

Olympia, WA14 days ago

$178,300–$407,000 Per Year

If you have a disability and either need assistance applying online or need to request an accommodation during any part of the application process, please call 1-800-EY-HELP3, select Option 2 for candidate related inquiries, then select Option 1 for candidate queries and finally select Option 2 for candidates with an inquiry which will route you to EY's Talent Shared Services Team (TSS) or email the TSS at ssc.customersupport@ey.com . We are looking for a Senior Manager, Data Scientist to be a senior technical leader across our most important AI bets driving applied research, leading multi-disciplinary teams, and shaping how EY designs, builds, and scales AI solutions for our clients.

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Winter Research Jobs in Olympia, WA

Clinical Research Assistant II MultiCare Health System

State and Local Tax Associate (Fall 2027/Winter 2028) RSM US LLP

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Clinical Research Coordinator Sr MultiCare Health System

Clinical Research Assistant - Lacey Providence St. Joseph Health

Research Support Pharmacist MultiCare Health System

Research Associate The Evergreen State College

Senior Clinical Research Director (SCRD) The Henry M. Jackson Foundation

Clinical Research Coordinator II - Madigan AMC The Henry M. Jackson Foundation

Senior Clinical Research Associate/Clinical Research Associate II - Northeast, Southeast, Central U Parexel

Clinical Research Associate/Senior Clinical Research Associate- FSP Parexel

Senior Clinical Research Associate/Clinical Research Associate II - FSP Parexel

Clinical Research Associate II/Senior Clinical Research Associate - All US Locations - HEM/ONC - FS Parexel

Site and Monitoring Health Lead / Lead Clinical Research Associate - Northeast US - FSP Parexel

Senior Clinical Policy Research Professional Humana

Senior Clinical Research Associate - Oncology - Florida - FSP Parexel

Senior Clinical Research Associate - Midwest/Central US - FSP Parexel

Business Tax Services - Federal Tax Advisory - Research & Credits Senior Manager EDGE EY

Clinical Research Coordinator II Metis Foundation

Senior Medical Director - Clinical Research Pharming Healthcare

Senior Medical Director, Clinical Research (Ophthalmology) Sumitomo Pharma

Director, Clinical Research Sumitomo Pharma

Senior Medical Director, Clinical Research Neurology Sumitomo Pharma

Context Engineer - Manager - Consulting - Location OPEN EY

Monitoring Team Lead / Senior Monitoring Team Lead United Therapeutics

Spanish Bilingual Registered Dietician Clinical Trials Telehealth - Per Diem - Washington IQVIA

Senior Director, Clinical Development - Antibacterials, Antifungals, CMV & Covid 19 Merck

Clinical Manager, Gastroenterology (GI) Customer Success Cardinal Health

Data Scientist - Senior Manager- Consulting - Location OPEN EY

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