Tacoma Community CollegeAssociate Vice President - Human Resources Tacoma Community CollegeAssociate Vice President - Human ResourcesTacoma WA 98466, WA, WA$150,000–$165,000 / yearJob Description:The Associate Vice President for Human Resources (AVP-HR) serves as a strategic, operational, and human resources leader, playing a crucial role in creating and implementing a human resources department that aligns with the College's goals, values, and strategic plan, and addresses the diverse needs of the workforce. Moreover, TCC stands in solidarity with Black Lives Matter and the Black community by further strengthening collaboration with the Black Student Union as well as community entities such as the Tacoma-Pierce County Black Collective, the Tacoma Urban League, and local black-owned businesses.
Tacoma Community CollegeTitan PULSE Mentor Tacoma Community CollegeTitan PULSE MentorTacoma WA 98466, WA, WA$20–$20 / hourAccording to the Community College Survey of Student Engagement, TCC ranks high on measures of active and collaborative learning and support for learners, thanks to our creative and effective staff and faculty. Inclusion: The TPM will demonstrate a commitment to inclusion in the following ways: Participate and engage in departmental trainings and continued learning o the subject of diversity, equity, and inclusion.
Columbia DistributingDirector of External Affairs - Kent, WA Columbia DistributingDirector of External Affairs - Kent, WAWoodmont Beach, WA$115,000–$135,000 / yearFull timeThe Director of External Affairs will serve as a strategic partner to the Vice President of External Affairs & Communications, helping to shape and support Columbia Distributing's engagement and communications strategy. The Director will serve as an important bridge between the company and key stakeholders, including teammates, media, community organizations, suppliers, retail partners, industry associations, and policymakers.
DaVitaState Government Affairs Sr Director DaVitaState Government Affairs Sr DirectorFederal Way, WAFull timeQualified candidates will have 10+ years of strong public policy and/or corporate government affairs experience at the state legislative or regulatory environment within with a demonstrated ability to independently lead highly-leveraged state advocacy campaigns/initiatives. Washington Non-exempt: Bellingham: $19.13/hour, Burien: $21.63/hour, Everette: $20.77/hour, Unincorporated King County: $20.82/hour, Renton: $21.57/hour, Seattle: $21.30/hour, Tukwila: $21.65/hour, Remainder of Washington state: $17.13/hour.
Bausch + LombDirector, Regulatory Affairs Bausch + LombDirector, Regulatory AffairsTacoma, WA$165,000–$220,000 / yearQualifications: + Bachelors degree required; advanced degree (Masters, PhD, PharmD) preferred + 10-15+ years in Regulatory Affairs or relevant experience in a regulated environment + Global portfolio management and strategy experience and strong familiarity with registration requirements in exU.S. The Director partners crossfunctionally with Clinical, Nonclinical, CMC, Quality, Safety, and Regulatory Operations to develop global regulatory strategies, lead health authority interactions, ensure highquality submissions, and manage regulatory risk across the product lifecycle.
ParexelRegulatory Affairs Consultant - Clinical Regulatory Affairs ParexelRegulatory Affairs Consultant - Clinical Regulatory AffairsOlympia, WAExperience with other global Health Authorities and applicable regulations are strongly preferred + Project management / leadership experience + Excellent interpersonal and intercultural communication skills, both written and verbal + Client-focused approach to work (Quality) + Results orientation + Teamwork and collaboration skills + Consulting skills + Critical thinking and problem-solving skills + Proficiency in local language and extensive working knowledge of the English language Why Join Parexel? You'll serve as the primary regulatory expert across multiple clinical studies, working shoulder-to-shoulder with cross-functional teams and client stakeholders to enable compliant, efficient trial execution.
ParexelSenior Regulatory Affairs Consultant - Regulatory Intelligence (Talent Pool) ParexelSenior Regulatory Affairs Consultant - Regulatory Intelligence (Talent Pool)Olympia, WAConsultant, you will: + Regularly search the public domain for new and updated regulations and regulatory guidance documents that can impact the client's development programs, and report the most critical findings + Regularly search the public domain for competitor product regulatory developments and report the most critical findings + Inform client immediately of any changes to the regulatory environment directly affecting client's business + Search for non-compliance letters or notices for client's suppliers and provide a regular report + Perform ad hoc research on specific regulatory topics at client's request, using the internet and various subscription database tools + Identify public commenting opportunities for draft guidances/regulations and coordinate review and comments from client. In this consultative role, you will combine regulatory expertise, analytical rigor, and strong project leadership skills to navigate an evolving regulatory landscape while collaborating closely with clients, internal experts, and global teams.
OracleNewMedical Device Regulatory Affairs Strategist OracleMedical Device Regulatory Affairs StrategistOlympia, WARemote$87,000–$178,100 / yearJob Description** **Lead/Principal/Senior Regulatory Affairs Specialist - Health & Life Sciences Legal and Compliance Group** Location: Remote/telecommuting from with the US (with preference for the east coast) **About the Role:** At a time when global technological developments and healthcare regulations are occurring and changing at an unprecedented rate, the success of large, complex global health companies requires regulatory leaders who are deeply steeped in the public and private levers that impact this industry. As a Principal/Lead/Senior Regulatory Affairs Specialist, you will work in collaboration with product engineering and development teams and subject matter experts on the total product lifecycle of AI-enabled, Cloud-native software applications used in clinical operation, clinical information systems, and clinical decision support (medical device and non-medical Device).
ParexelSenior Regulatory Affairs Consultant - Ad Promo ParexelSenior Regulatory Affairs Consultant - Ad PromoOlympia, WASenior Regulatory Consultant - Advertising & Promotion (Strategic Lead) We are seeking a highly strategic and experienced Senior Regulatory Consultant - Advertising & Promotion to serve as a trusted advisor across cross-functional teams. This role extends beyond execution, requiring a proactive leader who can independently review materials, interpret evolving FDA guidance, and pivot regulatory strategy to support business objectives while mitigating risk.
Otsuka America Pharmaceutical Inc.Senior Manager, Global Regulatory Affairs Otsuka America Pharmaceutical Inc.Senior Manager, Global Regulatory AffairsOlympia, WAPosition Summary** Provides critical support in developing global regulatory strategy, planning and execution of global investigational and marketed prescription drug submissions and manages lifecycle activities for all assigned projects in alignment with the Global Regulatory Lead. **J** **ob Responsibilities** - Provides critical support in developing global regulatory strategy, planning and execution of global investigational and marketed prescription drug submissions and manages lifecycle regulatory activities in alignment with the Global Regulatory Lead (GRL).
United TherapeuticsAssociate Corporate Compliance Director - Commercial & Medical Affairs United TherapeuticsAssociate Corporate Compliance Director - Commercial & Medical AffairsOlympia, WA$145,500–$205,000 / yearWho You Are The Associate Corporate Compliance Director reports to the Senior Corporate Compliance Director and serves as a key compliance business partner to Commercial and Medical Affairs, including Sales, Marketing, Commercial Training and Development, Patient Advocacy, and Medical Affairs. 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.
John DeereManager, Government Affairs John DeereManager, Government AffairsOlympia, WARemoteYour Responsibilities** As a **Manager, Government Affairs** for **John Deere** , located in the western United States, you will: + Monitor legislative and regulatory developments and identify specific initiatives that present opportunities or threats to company interests. + Alert Corporate and Business Unit management of pending legislative and regulatory initiatives, and develop strategies and action plans, in concert with business units, for affecting changes in policy and advance the Company's interests.
Canon USA & AffiliatesLeader Medical Affairs Canon USA & AffiliatesLeader Medical AffairsOlympia, WARemote10 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. Analyze and communicate technical and clinical product specification requirements from luminaries, market research teams, and via Medical Advisory Boards (MABs) to global business team.
Olympia Federal SavingsMarketing and Communications Coordinator Olympia Federal SavingsMarketing and Communications CoordinatorOlympia, WA$26.09–$39.13 / hourFull timeDevelop messaging strategy for digital marketing initiatives including customer email campaigns, in-branch broadcast screens, online banking advertising, texting initiatives, video content, and podcast production. Proficiency with website content management systems, social media platforms, email marketing platforms, podcast production tools, graphic design programs, video editing software, and MS.
DaVitaSurvey Outcome Manager DaVitaSurvey Outcome ManagerFederal Way, WARemoteFull timeWashington Non-exempt: Bellingham: $19.13/hour, Burien: $21.63/hour, Everette: $20.77/hour, Unincorporated King County: $20.82/hour, Renton: $21.57/hour, Seattle: $21.30/hour, Tukwila: $21.65/hour, Remainder of Washington state: $17.13/hour. New York Non-exempt: New York City and Long Island: $17.00/hour, Nassau, Suffolk, and Westchester counties: $17.00/hour, Remainder of New York state: $16.00/hour.
CoinbaseCommunications Manager, Policy & Public Affairs CoinbaseCommunications Manager, Policy & Public AffairsOlympia, WA$170,000–$200,900 / yearOur full notice outlining how data will be processed as part of the application procedure for applicable locations is available https://www.coinbase.com/legal/application-arbitration-agreement *AI Disclosure* For select roles, Coinbase is piloting an AI tool based on machine learning technologies to conduct initial screening interviews to qualified applicants. * Demonstrates the ability to responsibly use generative AI tools and copilots (e.g., LibreChat, Gemini, Glean) in daily workflows, continuously learn as tools evolve, and apply human-in-the-loop practices to deliver business-ready outputs and drive measurable improvements in efficiency, cost, and quality.
Washington State Insurance CommissionerNewPolicy and Rules Manager Washington State Insurance CommissionerPolicy and Rules ManagerOlympia, WA$105,000–$140,000 / yearFull timeYou will serve as a subject matter expert on legislative and administrative rulemaking processes, provide strategic guidance to agency leadership, and collaborate with stakeholders across the agency and state government to advance consumer-focused policy solutions. The Washington State Office of the Insurance Commissioner (OIC) is seeking a strategic and collaborative Policy and Rules Manager to help advance our mission of protecting consumers, the public interest, and Washington's economy through fair and efficient regulation of the insurance industry.
Washington State Insurance CommissionerNewInvestigator 3 (Investigator 2 In-Training) Washington State Insurance CommissionerInvestigator 3 (Investigator 2 In-Training)Tumwater, WA$5,812–$6,414 / monthFull timeThe in-training opportunity allows you to grow from a senior investigator role into an expert-level investigator, expanding your expertise in regulatory investigations, enforcement support, and administrative proceedings. The Office of the Insurance Commissioner (OIC) is seeking an Investigator 2 In-Training to Investigator 3, or an Investigator 3 to join our Regulatory Investigations Unit within the Legal Affairs Division.
Olympia Federal SavingsCommercial Loan Officer II Olympia Federal SavingsCommercial Loan Officer IILacey, WA$88,849–$144,380 / yearFull timeAnalyze, evaluate, and prepare tax analysis cash flow reports on commercial loan and multiple non-owner-occupied loan guarantors that exceed aggregate loan balance limits. KNOWLEDGE, SKILLS AND ABILITY REQUIREMENTS: Excellent public and customer relations skills to effectively communicate with internal and external customers, determine their needs, and maintain their confidence.
Olympia Federal SavingsCommercial Loan Officer III Olympia Federal SavingsCommercial Loan Officer IIILacey, WA$102,177–$166,038 / yearFull timeAnalyze, evaluate, and prepare tax analysis cash flow reports on commercial loan and multiple non-owner-occupied loan guarantors that exceed aggregate loan balance limits. KNOWLEDGE, SKILLS AND ABILITY REQUIREMENTS: Excellent public and customer relations skills to effectively communicate with internal and external customers, determine their needs, and maintain their confidence.
FujifilmDir of US Govt Affairs-Federal FujifilmDir of US Govt Affairs-FederalOlympia, WA$130,491–$228,000 / yearCurrent lobbying experience and registration is required** **with experience lobbying in the semiconductor or global trade field** **.** This role reports to the Head of Government Affairs and operates in a remote capacity while coordinating efforts across multiple business units. The ideal candidate will possess deep expertise in lobbying Congress and the Executive Branch, with a proven track record in advocating on complex policy issues, driving legislative outcomes, and building influential relationships with key policymakers.
Sumitomo PharmaDirector, Regulatory Advertising & Promotion Sumitomo PharmaDirector, Regulatory Advertising & PromotionOlympia, WA$187,520–$234,400 / yearSumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. Key Core Competencies + Strong verbal and written communication skills; interpersonal skills; listening skills; and organizational skills with the ability to influence others, internally and externally, in a positive and effective manner.
Cardinal HealthNewRegulatory Scientist III Cardinal HealthRegulatory Scientist IIIOlympia, WAWe currently have a career opening for a Regulatory Scientist III **What Chemistry, Manufacturing and Controls contributes to Cardinal Health** The Scientist III in CMC is a senior-level contributor responsible for leading regulatory strategy and execution for pre-approval, post-approval changes and lifecycle management activities across client Rx and non-Rx programs. Operating in a client-facing, consultant capacity, this role provides strategic guidance on complex regulatory submissions, authors and reviews high-impact documentation, and drives alignment across cross-functional teams to ensure successful regulatory outcomes.
OracleNewSenior Regulatory Program Manager OracleSenior Regulatory Program ManagerOlympia, WA$79,100–$166,100 / yearJob Description** **Senior Regulatory Program Manager** **Location:** Telecommuting/remote from within the US (eastern/central time zone ideal) At a time when global technological developments and healthcare regulations are occurring and changing at an unprecedented rate, the success of large global health companies require experienced regulatory leaders who can navigate complex and fast-changing regulations, and public policies across the globe. As Program Manager on the Health and Life Sciences Legal and Compliance Team, you will work in collaboration with Product teams and subject matter experts to compile, track, and organize the required documentation to register products in global markets where the products are sold.
City of Tacoma WARegulatory Compliance Analyst, Senior City of Tacoma WARegulatory Compliance Analyst, SeniorTacoma, WA$98,280–$138,320 / yearRegulatory Compliance Analyst, Senior Salary $98,280.00 - $138,320.00 Annually Location Tacoma, WA Job Type Classified Job Number P1600-26A Department City of Tacoma - CITY WIDE LIST Opening Date 05/28/2026 Closing Date 6/10/2026 5:00 PM Pacific + Description + Benefits + Questions Position Description Are you passionate about environmental stewardship, public service, and making a lasting impact in the communities you serve? The City of Tacoma provides excellent medical, dental and vision plans for the whole family; paid holidays and paid leave; participation in the Tacoma Employees' Retirement System (alternate plan for Police/Fire); continuing education and advancement opportunities and a growing variety of City-sponsored health and wellness opportunities and incentives.
Otsuka America Pharmaceutical Inc.Associate Director, R&D HCP Engagement Otsuka America Pharmaceutical Inc.Associate Director, R&D HCP EngagementOlympia, WA$6–$8 / hourJob Summary** The Associate Director, R&D HCP Engagement CoE is a critical change agent and system implementer responsible for designing the operating model and overseeing the execution of a unified, compliant, and exceptional service model for all Healthcare Professional (HCP) engagement and contracting within R&D. **Governance, Compliance, and Audit Readiness** + Serve as the primary point of accountability for global oversight of HCP interactions, ensuring compliance with internal policies, legal requirements, and industry codes (e.g., PhRMA, EFPIA).
Otsuka America Pharmaceutical Inc.Medical Director, Global Medical Strategy Otsuka America Pharmaceutical Inc.Medical Director, Global Medical StrategyOlympia, WACross-Functional Collaboration: Collaborate closely with other key functions, including regional medical leads, clinical development, global value and real-world evidence, US and global commercial teams, market access, and regulatory affairs, to ensure integrated global strategies and cohesive medical affairs strategies and input into cross functional leadership meetings and plans. As we continue to develop innovative medicines for those with CNS disorders, we are seeking a skilled and experienced Medical Director of CNS Early Assets, Global Medical Affairs, responsible for certain assets within the broader CNS TA portfolio Medical Affairs (both US and Global), with a specialization in Psychiatry and/or Neurology.
Otsuka America Pharmaceutical Inc.Associate Director, Global Labeling Otsuka America Pharmaceutical Inc.Associate Director, Global LabelingOlympia, WAEffective written and oral communication and organizational skills + Strong attention to detail + Solid aptitude for use of IT systems; preferable knowledge with Regulatory Information Management System (RIMS) and electronic document management system (EDMS); Proficiency in MS Office suite; Willing to learn additional applications + Ability to think strategically, communicate risks, and recommend problem solving innovative solutions + Ability to recognize and escalate issues + The ideal candidate should be action oriented, customer focused, ability to manage workloads and set priorities. Preferred **Knowledge and skills** + Solid understanding and practical knowledge of labeling regulatory requirements, regulations and guidance required + Solid understanding of implications of global labeling across the organization and globally + Solid understanding of the structure of product labeling + Experience in effectively/appropriately prioritizing and managing multiple high to medium complex projects simultaneously + Ability to work independently or in teams, globally.
Otsuka America Pharmaceutical Inc.Associate Director, Scientific Communications - CNS Otsuka America Pharmaceutical Inc.Associate Director, Scientific Communications - CNSOlympia, WAMonitor and analyze content performance and stakeholder feedback to inform future content strategy and optimization + Consider technology and AI to support workflow improvement **Scientific Narrative Ownership** + Manage and provide direction for the core scientific lexicon and messaging, ensuring its consistent application across all Medical Affairs materials through clear guidance to the Manager of Core Content **Cross-Functional Collaboration** + Partner closely with Clinical Development, Global Integrated Evidence & Innovation, and Regulatory teams to gather and accurately interpret new data, ensuring the Manager of Core Content applies this information consistently and accurately into communication materials + Support the US Field Medical Affairs Lead by ensuring the Manager of Core Content develops and maintains a high-quality, scientifically rigorous, and compliant content repository for the field team + Manage the operational execution and day-to-day budget for external medical writing and communications agencies that support content and publication deliverables **Qualifications:** **Education and Experience** + Advanced scientific degree is required (PharmD, MD, PhD, or equivalent) with a strong understanding of clinical development and medical science, preferably in the relevant therapeutic area. **Skills and Competencies** + Demonstrated ability to provide guidance, coaching, and mentorship to a direct report, delegate tasks effectively, and maintain accountability for project quality + Exceptional ability to interpret complex clinical and scientific data and apply it consistently and accurately across communication materials + Strong ability to navigating complex data and evolving treatment paradigms in psychiatry and neurology + Strong organizational skills with the ability to manage multiple simultaneous project workflows (content and publications) and drives improvements to development processes + Excellent interpersonal skills with the ability to communicate scientific strategy clearly to both internal experts and external vendors/authors & tailor communications to address unique challenges in the relevant therapeutic area (e.g., stigma, patient diversity, long-term outcomes).
Otsuka America Pharmaceutical Inc.Associate Director, Global Quality Operations Otsuka America Pharmaceutical Inc.Associate Director, Global Quality OperationsOlympia, WAMinimum $150,034.00 - Maximum $224,250.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States. **Global Quality System Processes** + Oversee the design, implementation, and maintenance of global quality system processes (e.g., deviation management, CAPA, change control, document management) guided by process excellence principles.
Bausch + LombSenior Director, Head of Trademarks Bausch + LombSenior Director, Head of TrademarksOlympia, WA$280,000–$320,000 / yearResponsibilities:** **Portfolio leadership** + Own and manage a large global trademark portfolio encompassing pharmaceutical product names, consumer brand marks, trade dress, and device/surgical brands across 100+ jurisdictions. 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.
Pharming HealthcareSenior Director - Labeling and Operations Pharming HealthcareSenior Director - Labeling and OperationsOlympia, WARemote$230,000–$290,000 / yearQualifications** + Bachelor of Science degree in a life sciences or technical field from an accredited university; advanced scientific-related degree preferred + RAC Certification preferred + In depth knowledge of global regulatory affairs requirements for pharmaceuticals and biologics + A minimum 15 years related experience in Global Regulatory Affairs + At least 10 years of experience involving global labeling operations, development and maintenance + At least 5 years of experience involving the direct implementation of promotional labeling and advertising regulations in the biotech/pharmaceutical industry globally; this must include experience providing regulatory input and evaluation as part of a promotional review committee + Excellent oral and written communication skills are a must, as are superior planning skills + Detailed-oriented, self-motivated, and be comfortable with broad responsibilities in a fast-paced environment + Ability to travel as needed both domestic and internationally (average of one trip per quarter) + 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. We are looking for talented individuals who are excited about living our values: + We put Patients at the heart + We act with urgency + We get it done + We make it simple **Our Vision** Our Vision is to develop a leading global rare disease company with a diverse portfolio and presence in large markets, leveraging proven and efficient clinical development, supply chain, and commercial infrastructure.
Otsuka America Pharmaceutical Inc.NewMedical Science Liaison, CNS - KY, South OH, WV Otsuka America Pharmaceutical Inc.Medical Science Liaison, CNS - KY, South OH, WVOlympia, WABuild, cultivate, and leverage external relationships with key scientific and medical customers and organizations within their ecosystem to ensure strong understanding of evolving healthcare trends, disease state, Otsuka products, systems, and services across the ecosystem landscape, including KIs, LPLs, Key Decision Makers (KDMs) and Patient Advocacy. + Assist with Otsuka's clinical trials program, including registrational, post-marketing and Investigator-Sponsored Trials (ISTs), health economic outcomes research, other specific medical collaborations; provide clinical expertise and feedback regarding operational management of clinical trials to ensure optimal site selection and performance.
Otsuka America Pharmaceutical Inc.Director, Global Clinical Development Otsuka America Pharmaceutical Inc.Director, Global Clinical DevelopmentOlympia, WADetailed Description of Duties:** - Otsuka is seeking a Director, Global Clinical Development (GCD) based Remotely or in our Princeton, NJ or Rockville, MD offices, who will be responsible for the design and oversight of clinical research programs and protocols for OPDC products under good clinical practices (GCP). Minimum $209,599.00 - Maximum $313,375.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States.
Cardinal HealthManager, Sustainable Supply Chain Cardinal HealthManager, Sustainable Supply ChainOlympia, WA$105,500–$150,100 / yearRESPONSIBILITIES** **Sustainable Supply Chain Strategy & Execution** + Develop responsible sourcing strategies, align with internal stakeholders to gain strategic alignment between responsible sourcing and business objectives, and implement and enforce related policies and procedures + Function as the subject matter expert to inform Cardinal Health's approach to human rights and ethical supplier engagement and due diligence + Manage sustainability supply chain mapping to increase transparency and traceability across Cardinal Health's supplier base. This Manager will lead our responsible sourcing program, function as the subject matter expert on human rights and ethical supplier engagement strategies, help Cardinal Health to meet our science-based climate target, drive emissions reduction across the pharmaceutical and healthcare supply chain, and support compliance with growing legislation worldwide.
MerckNewClinical Director, Clinical Research, Ophthalmology MerckClinical Director, Clinical Research, OphthalmologyOlympia, WA$255,800–$402,700 / yearJob Responsibilities** + Specifically, the Clinical Director may be responsible for: + Planning clinical trials (designing, collaborating on operational plans, etc.) based on the clinical development strategy + Medical oversight and overall conduct of ongoing or new clinical trials for investigational or marketed drugs + Analyzing and summarizing clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication + Participating in internal and joint internal/external research project teams relevant to the development of new compounds, and the further study of marketed compounds + Supporting business development assessments of external opportunities The Clinical Director may: + Actively engage with other functional areas in support of study execution + Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and + Assist the team in ensuring that other colleagues are informed of the progress of studies of our company and competitors' drugs, and + Provide expert opinion, internally and externally, on relevant scientific questions within their responsibility. The Clinical Director is responsible for maintaining a strong scientific fund of knowledge by: + Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies + Identifying scientifically and operationally strong investigators who can assist in the development of our company's investigational and marketed drugs + Establishing communications with prominent clinical investigators in his/her particular field of interest, particularly those who will be willing and able to assist in the evaluation of our company's drugs + Attending appropriate scientific meetings to maintain his or her competency and to maintain awareness of research activities in his/her area of responsibility.
HumanaNewSenior Compliance Professional HumanaSenior Compliance ProfessionalOlympia, WARemote$86,300–$118,700 / yearUse your skills to make an impact** **Required Qualifications** + Bachelor's degree in business, data analytics, or IT + 3 or more years of experience in healthcare or a healthcare related industry + Knowledge/understanding of laws and regulations governed by the Department of Insurance and CMS + Reporting experience with external partners (DOI, CMS, DoD) + Experience in working with large data sets **Preferred Qualifications** + Graduate or advanced degree + Audit or consulting experience + Experience within a metric intensive organization Additional information In this role you will be an individual contributor. Additional responsibilities includes coordination with Regulatory Compliance for government regulator (or their contracted vendors) communications as well as internal coordination with Corporate Affairs and other business partners regarding issues or other concerns/barriers related to timely submission of accurate and complete data.
CognizantVeeva Vault RIM Test & Validation Lead (CSV / QEA) CognizantVeeva Vault RIM Test & Validation Lead (CSV / QEA)Olympia, WA$71,100–$112,500 / yearAbout the role** As a **Veeva Vault RIM Test & Validation Lead (CSV / QEA)** , you will make an impact by driving validation strategy and ensuring compliance of regulatory systems supporting global submissions. Think about your transferable experiences and unique skills that make you stand out as someone who can bring new and innovative ideas to this role.
GovernmentJobs.comNewEXECUTIVE DIRECTOR GovernmentJobs.comEXECUTIVE DIRECTORAuburn, WABuild and maintain relationships with key partners including but not limited to: Commissioners, criminal justice agency leaders and representatives, Tribes and tribal enforcement agencies, community groups and their members, elected officials and their staff, other state agencies and offices such as the Office of Financial Management (OFM) and the Attorney General's office, professional associations such as WASPC, IADLEST, and many others. Demonstrated strong criminal justice leadership experience including various specialty assignments, multi-agency task forces, multi-disciplinary programs, investigative or regulatory programs, project teams, or the like is required to understand the interconnected roles of the fields for which training is provided and the way in which the criminal justice system operates.
Otsuka America Pharmaceutical Inc.NewDirector, Statistics Otsuka America Pharmaceutical Inc.Director, StatisticsOlympia, WAThis role will lead statistical innovation and data insights in HTA and Integrated Evidence Plan (IEP), including efficient statistical design and execution of late-phase clinical trials and real-world studies, AI/ML-based population enrichment, Bayesian methods, RWD/external control, and collaborate closely with cross-functional teams including Global Value Evidence, Global Medical Affairs, Market Access, Regulatory, Biostatistics, Global Clinical Development and Clinical Management. Otsuka is seeking an experienced Director of Statistics to join our Data Science and AI group to provide statistical leadership and solutions to efficient phase 3b/4/Real-World-Evidence (RWE) study design, global Health Technology Assessment (HTA) and regulatory requirements on advanced statistics needs for our portfolio across therapeutic areas and indications.
Mineralys Therapeutics IncNewRegional Sales Director - Northwest Mineralys Therapeutics IncRegional Sales Director - NorthwestNorthwest, WARemote$180,000–$215,000 / yearMineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities such as chronic kidney disease (CKD), obstructive sleep apnea (OSA) and other diseases driven by dysregulated aldosterone. This leader will be accountable for translating national strategy into regional execution, driving business performance through strong field leadership, cross-functional partnership, and disciplined execution against launch objectives.
Otsuka America Pharmaceutical Inc.Senior Director, Global Clinical Development - Nephrology & Immunology Otsuka America Pharmaceutical Inc.Senior Director, Global Clinical Development - Nephrology & ImmunologyOlympia, WADemonstrated experience in all developmental phases including evaluation of pre-clinical or in licensing candidates' potential for meeting an unmet medical need, establishing early clinical safety and proof of concept, conduct of global trials for registration, and implementation of late stage life-cycle management strategies, - Demonstrated experience in successfully leading clinical aspects of regulatory interactions; experience with a successful regulatory filing is a plus. - Contributes to corporate initiatives by participating in continuous process improvement to meet company **Knowledge, Skills, Competencies, Education, and Experience** **Required:** - A clinician (M.D., or D.O.) preferably with an immunology, rheumatology, or dermatology background including management experience (direct or indirect).
Washington Association for Community HealthDirector of Policy & Advocacy - Hybrid Washington Association for Community HealthDirector of Policy & Advocacy - HybridOlympia, WA$90,402–$144,602 / yearThe Director of Policy & Government Affairs plans, manages, and implements the Association's policy, government affairs, and advocacy programs, representing and elevating the Association's presence before state and federal legislative and administrative bodies within the health and healthcare sectors in Washington. With support from the CEO, creates and implements a comprehensive, year-round policy, government affairs and advocacy strategy that increases the Association's presence with state and federal leaders, through oversight of all efforts related to advocacy, community organizing, research, and policy analysis initiatives.
Pharming HealthcareSenior Medical Director - Clinical Research Pharming HealthcareSenior Medical Director - Clinical ResearchOlympia, WARemote$310,000–$375,000 / yearParticipate in strategic planning as part of Medical Affairs, Marketing and Business Development teams + Provide medical and scientific leadership and support at key scientific meetings (US and International) + Extensive interactions with academic thought leaders to optimize and develop clinical trial strategies + Perform other duties as assigned **Qualifications** + Medical license in good standing in a U.S. State or Territory preferred + 5+ years in clinical development including managing CROs + Experience in product launch, regulatory filings and FDA communications highly preferred + Strong leadership and management skills + Strong verbal and written communication skills are essential + Exceptional interpersonal skills and problem-solving capabilities + Ability to work effectively across a global matrixed organization + Travel - Include 20% travel time required for the position where travel occurs locally or internationally, if applicable + Commitment and alignment to Pharming's mission, core values and behaviors **Salary Range** Pharming takes into consideration a combination of candidate's work experience, training, and education, as well as the scope of the role, complexity, and external market and internal value when determining a salary level. **Responsibilities** + Lead/support clinical development (strategy, develop protocols, study start-up, close-out, oversight, and regulatory support) for napazimone studies + Dedicated medical and scientific role to execute of the clinical strategy for the napazimone program, including + Support the pivotal napazimone studies for mtDNA Primary Mitochondrial Disease + Lead the napazimone pediatric study plan and clinical pharmacology studies + Lead the napazimone program for new indications + Work cross-functionally to define, plan, and implement studies + Lead the sponsor oversight of medical monitoring across the napazimone programs + Analyze and oversee data from clinical trials and produce reports, including safety data, efficacy data, completeness and trend analysis eCRF data, and oversight of protocol deviations + Lead clinical study site engagement in the US + Participating and providing clinical input into safety and regulatory interactions.
Metis FoundationClinical Research Coordinator II Metis FoundationClinical Research Coordinator IIJoint Base Lewis-McChord, WA$60,000–$70,000The overall purpose of this study is to conduct, in collaboration with multiple Defense Health Agency sites and external collaborators, the development of a biosensor that will eventually be capable of integrating into a system comprising biosensors, respiratory risk assessment software, and healthy building controls to mitigate bioaerosol-related respiratory illnesses in military healthcare facilities. Assist relevant team members with the coordination of regulatory requirements such as protocol amendments, reportable events, writing informed consent forms and HIPAA forms, writing annual reports and IRB continuing reviews, and address stipulations issued from IRB to reach approval, while keeping investigators apprised of changes.
Otsuka America Pharmaceutical Inc.Director, Global Quality GMP Processes Otsuka America Pharmaceutical Inc.Director, Global Quality GMP ProcessesOlympia, WAKey Responsibilities** + Global Process Ownership: Lead the design, implementation, and continuous improvement of global quality processes for: + Product Quality Complaints + Corrective and Preventive Actions (CAPA) + Deviations + Management Reporting and Trending + Benchmarking & Best Practices: Evaluate internal and external quality practices to identify and implement best-in-class solutions that enhance compliance and operational efficiency. Minimum $186,489.00 - Maximum $278,875.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States.
Otsuka America Pharmaceutical Inc.Director, Clinical Management (Immunology/Biologics/Cell Therapy) Otsuka America Pharmaceutical Inc.Director, Clinical Management (Immunology/Biologics/Cell Therapy)Olympia, WAExperience in immunology/biologics/cell therapy is strongly preferred - Experience with complex basket trials is also preferred Educational Qualification Required: - Bachelor's Degree with a minimum of 14 years of applicable pharmaceutical industry experience including 10 years clinical trial management experience. **Job Summary** In collaboration with the Senior Director of Clinical Management, the Director is responsible for the operational strategy and management of Otsuka clinical programs, including coordination with other relevant parties (e.g., other Otsuka departments, external service providers (ESPs), etc.).
Otsuka America Pharmaceutical Inc.Director, Clinical Management Early Phase, CNS Otsuka America Pharmaceutical Inc.Director, Clinical Management Early Phase, CNSOlympia, WAJob Summary** In collaboration with the Senior Director of Clinical Management, the Director is responsible for the operational strategy and management of Otsuka clinical programs, including coordination with other relevant parties (e.g., other Otsuka departments, external service providers (ESPs), etc.). Minimum $186,489.00 - Maximum $278,875.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States.
MerckSenior Director, Clinical Development - Antibacterials, Antifungals, CMV & Covid 19 MerckSenior Director, Clinical Development - Antibacterials, Antifungals, CMV & Covid 19Olympia, WA$282,200–$444,200 / yearRole may be remote **Specifically, the Senior Director may be responsible for:** · Planning clinical trials (design, operational plans) based on the clinical development strategies for investigational or marketed infectious disease drugs · Monitoring and managing the conduct of ongoing or new clinical trials for investigational or marketed infectious disease drugs · Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publications · Participation in internal and joint internal/external research project teams relevant to the development of investigational drugs, and the further study of marketed drugs · Developing clinical development strategies for investigational or marketed infectious disease drugs · Presenting study data and program strategic plans to internal governance committees for endorsement and key program milestones **The Senior Director is responsible for maintaining a strong scientific fund of knowledge by:** · Maintaining awareness of scientific developments within their area of expertise, including new scientific findings and research methodologies · Establishing communications with prominent clinical investigators in their particular field of interest, particularly those scientifically and operationally strong investigators who can assist in the development of our company's investigational and marketed drugs · Attending appropriate scientific meetings to maintain their competency and to maintain awareness of research activities in their area of responsibility. **To accomplish these goals, the Senior Director may:** · Author detailed development documents and presentations for internal and external audiences · Author scientific publications · Facilitate collaborations with external researchers around the world · Travel on company business up to about 10% of the time to manage future or ongoing clinical research projects.
Gilead Sciences, Inc.Medical Scientist- Washington and Alaska Gilead Sciences, Inc.Medical Scientist- Washington and AlaskaOlympia, WA$165,495–$214,170 / yearResponsibilities** + Deliver timely, accurate, and succinct clinical, scientific, and educational presentations to healthcare providers in HIV Treatment and Prevention, both proactively and in response to requests for information, consistent with PhRMA guidelines, and FDA regulatory requirements + Implement defined goals and objectives aligned with the Medical Affairs Plan of Action and other strategic initiatives + Develop strategic plans for cultivating and maintaining working relationships with existing and future thought leaders in the assigned region + Provide timely insights to the strategy and competitive intelligence teams regarding treatment practice and trends observed in field interactions. The incumbent is an experienced, well-organized, results-oriented healthcare professional who will develop ongoing professional relationships related to HIV Treatment and Prevention and provide scientific support to key healthcare decision-makers in, public health and academic institutions, along with community and community healthcare providers throughout the assigned geography.