56 Results for

Research Jobs in Centralia, WA

Jobs

Joint Base Lewis-McChord, Washington11 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.

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.

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.

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.

Tumwater, WA29 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.

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, WA4 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, WA10 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, WA13 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, WA7 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.

New!

Olympia, WA1 day 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.

Joint Base Lewis-McChord, WA27 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, WA1 day 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, WA1 day 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) .

Olympia, WA8 days ago

Rockstar 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.

New!

Olympia, WA3 days ago

The 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.

Olympia, WA29 days ago

Subject 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.

Olympia, WA28 days ago

$150,000–$200,000 Per Year

The 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.

Olympia, WA23 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_

New!

Olympia, WA1 day 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

Remote

$209,000–$238,500 Per Year

Basic 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.

New!

Olympia, WA2 days ago

$152,066–$202,755 Per Year

The Main Responsibilities** + Create and maintain a research plan grounded in Lumen's strategy and technological realities + Execute research, leveraging internal and external resources as appropriate, to develop insights and confirm or refute hypotheses about the changing nature of technology, business, government/public sector, entertainment, and sociocultural norms and their resulting impact on networking requirements + Synthesize research findings into research papers, blogs/articles, and other products meant for both technical and non-technical audiences + Effectively collaborate with Lumen product, engineering, marketing, and communications teams, among others + Monitor technological innovations and macro-trends, collaborate and share with researchers at other organizations **What We Look For in a Candidate** + Master's degree in Computer Science, Electrical Engineering, Telecommunications, Economics, Business, or related field; PhD preferred + Extensive experience in academic-style research planning, execution, and communication + Strong data analysis skills + Effective communication with senior teams (technical and non-technical) and excellent writing skills for a variety of audiences + Strategic thinking, an interest in business, and a thirst for what comes next + Self-motivated and proactive Preferred Qualifications: + PhD in Computer Science, Electrical Engineering, Telecommunications, Economics, Business, or related field + Experience in technology industries + Experience in B2B environments **Compensation** This information reflects the anticipated base salary range for this position based on current national data. Location Based Pay Ranges $152,066 - $202,755 in these states: AL AR AZ FL GA IA ID IN KS KY LA ME MO MS MT ND NE NM OH OK PA SC SD TN UT VT WI WV WY $159,670 - $212,893 in these states: CO HI MI MN NC NH NV OR RI $167,273 - $223,031 in these states: AK CA CT DC DE IL MA MD NJ NY TX VA WA Lumen offers a comprehensive package featuring a broad range of Health, Life, Voluntary Lifestyle benefits and other perks that enhance your physical, mental, emotional and financial wellbeing.

Olympia, WA30+ days ago

$79,100–$158,200 Per Year

Research 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.

Olympia, WA17 days ago

Remote

$90,000–$100,000 Per Year

What 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.

Olympia, WA30+ days ago

Develop and implement large-scale model architectures, leveraging model scaling and transfer learning techniques 2. Prioritize training scalability and signal scaling to optimize model performance, efficiency, and reliability 3. Develop and apply NextGen sequence learning techniques to drive advancements in recommender systems and machine learning 4. Design and implement generative modeling solutions for data augmentation 5. Collaborate with cross-functional teams to design and optimize ML systems, leveraging expertise in hardware-software co-design, including quantization, compression, and resource-efficient AI, to drive performance improvements and efficiency gains 7.

Olympia, WA15 days ago

Build and continuously refine evaluations for multimodal and agentic frontier AI models, including in cybersecurity, chemical security, and biosecurity 2. Build robust, reusable evaluation pipelines that scale across multiple model lines and product areas 3. Produce auditable technical artifacts, including evaluation reports and model cards, at high reliability and speed 4. Scope and deliver end-to-end evaluations under ambiguous and rapidly shifting requirements, re-prioritizing as the threat landscape and Meta's frontier models evolve 5. We ensure that evaluations are in place to mitigate these risks and responsibly handle the development of frontier AI.As a Research Engineer on Preparedness, you will work alongside world-class AI researchers to develop new evaluations grounded in real world threat models, maintain existing evaluations so they remain current and reliable, and produce written artifacts that Meta can trust during high-stakes launches.

Olympia, WA30+ days ago

Depending on your interests and strengths, your work could span post-training pipelines (SFT, RLHF, synthetic data generation), evaluation methodology (auto-judge design, benchmark construction, human-AI calibration), production serving systems (RAG, memory, multi-modal generation), multi-agent orchestration, or E2E experience of building agentic products, - all grounded in shipping to real users at scale **Required Skills:** AI Research Engineer Responsibilities: 1. Building a general-purpose agentic platform that powers a wide range of GenAI products across Facebook -enabling teams to ship faster, safer, and at scale.- Building systems that enable capacity and cost optimizations through model fine-tuning, post-training and other techniques.

Olympia, WA22 days ago

Remote

$146,700–$214,800 Per Year

Providecritical security focusedexpertisetoengineeringorganizations **Minimum Qualifications** + 3+ years of experience in vulnerability research or a closely related areasuch asexploitor mitigation developmentonLinuxSystems + 3+ years' experience with C/C++, and a scripting language (e.g., Python), and assembly (e.g., x86/x64, ARM, etc.) **Preferred Qualifications** + Bachelor's degree or equivalent in Computer Science, Electrical Engineering, Cyber Security, or other tech-related degree + Experience withLinux internals + Experience with binary auditing and reverse engineering, and with related tools such as IDA Pro, Binary Ninja,Ghidra, etc. and with plugin development. The applicable full salary ranges for this position, by specific state, are listed below: New York City Metro Area: $165,000.00 - $277,600.00 Non-Metro New York state & Washington state: $146,700.00 - $247,000.00 * For quota-based sales roles on Cisco's sales plan, the ranges provided in this posting include base pay and sales target incentive compensation combined.

Olympia, 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, WA7 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.

Olympia, WA9 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, WA15 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, WA30+ days ago

Responsibilities** : 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).

Olympia, WA14 days ago

10 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.

Olympia, WA30+ days ago

$190,800–$300,300 Per Year

Responsibilities and Primary Activities** **Scientific Exchange** + Develops professional relationships and engages with national and regional SLs to ensure access to company-approved medical and scientific information on areas of therapeutic interest and Company products + Conducts peer-to-peer scientific discussions and maintains a reliable presence with those SLs to ensure they have a medical contact within the company + Addresses scientific questions and directs SL inquiries on issues outside of RMSD scope (e.g., grants) to appropriate company resources consistent with applicable policies + Maintains current knowledge and comprehension of dynamic scientific and clinical environment in the Company's Areas of Interest (AOI) for the RMSD's specific therapeutic area. + Protocol lead responsibilities in collaboration with GCTO + Addresses questions from investigators and provides information regarding participation in Company-sponsored clinical studies **Scientific Congress Support** + Engages in scientific congresses and medical meetings, facilitates scientific and data exchange for both Company and competitor data.

Olympia, WA30+ days ago

$190,800–$300,300 Per Year

Olympia, WA30+ days ago

$190,800–$300,300 Per Year

Responsibilities and Primary Activities** **Scientific Exchange** + Develops professional relationships and engages with national and regional SLs to ensure access to company-approved medical and scientific information on areas of therapeutic interest and Company products + Conducts peer-to-peer scientific discussions and maintains a reliable presence with those SLs to ensure they have a medical contact within the company + Addresses scientific questions and directs SL inquiries on issues outside of Regional Medical Scientific Director scope (e.g., grants) to appropriate company resources consistent with applicable policies + Maintains current knowledge and comprehension of dynamic scientific and clinical environment in the Company's Areas of Interest (AOI) for the Regional Medical Scientific Director specific therapeutic area. + Protocol lead responsibilities in collaboration with GCTO + Addresses questions from investigators and provides information regarding participation in Company-sponsored clinical studies **Scientific Congress Support** + Engages in scientific congresses and medical meetings, facilitates scientific and data exchange for both Company and competitor data.

Olympia, WA30+ days ago

$190,800–$300,300 Per Year

Olympia, WA30+ days ago

$190,800–$300,300 Per Year

Olympia, WA10 days ago

$142,400–$224,100 Per Year

Inspection 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.

Olympia, WA30+ days ago

This 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.

Olympia, WA15 days ago

Remote

$173,200–$272,600 Per Year

Cross-Functional Collaboration (Matrix Leadership)** + Collaborate closely with Therapeutic Area Heads (Oncology), Clinical Development, Medical Affairs, and study teams/partners to shape alignment across scientific messaging, site engagement strategy, and operational execution across multiple oncology studies. **Job Description** The Clinical Liaison, Oncology reports to the Executive Clinical Research Director in Oncology and is a strategic, field-facing role within Global Clinical Trial Operations (GCTO) that bridges clinical execution and scientific engagement to accelerate patient recruitment and optimize trial delivery.

Olympia, WA9 days ago

$123,400–$176,300 Per Year

Work spans modern healthcare data platforms and AI engineering, including medallion architecture (bronze/silver/gold), Delta Lake, T-SQL ETL, and natural language AI capabilities such as NLP/NLU, retrieval-augmented generation (RAG), document-level LLM extraction, and agentic frameworks applied to EHR/EMR, practice management (PM), pharmacy, claims, and clinical note data. Specialty Networks' PPS Analytics platform analyzes data from electronic medical records (EMR), practice management, imaging, and dispensing systems and transforms it into meaningful and actionable insights for providers and other stakeholders by using artificial intelligence and modern data analytics capabilities.

Olympia, WA30+ days ago

Individuals 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.**

Olympia, WA7 days ago

Remote

Comply with departmental procedures and requirements, such as completion of project assignment and workload trackers on the applicable software platform + Analyze efficiency of work and discuss improvement ideas with Medical Writing + Services management and colleagues, e.g., evaluation of software to increase productivity and document quality. **Key Accountabilities** : **Author Clinical Documents** + Gather, review, analyze, and evaluate pertinent resources to prepare, develop, and finalize key clinical documents for submission to regulatory authorities, without the need for any supervision or additional formal on-the-job training.

Olympia, WA17 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, WA7 days ago

The 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.

Olympia, WA10 days ago

Remote

From innovative trial design, end-to-end biometrics to real-world evidence, value and access, we strive to shorten the drug development cycle and increase the probability of success, delivering better patient outcomes through our innovative analytical methods. A collaborative team player with strong industry experience who partners with Subject Matter Experts (SMEs) to enhance and update tools in response to evolving business needs.

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