Clinical Research Assistant - Lacey Providence St. Joseph HealthClinical Research Assistant - LaceyLacey, WAPart timeOur not-for-profit network also provides a full spectrum of care with leading-edge diagnostics and treatment, outpatient health centers, physician groups and clinics, numerous outreach programs, and hospice and home care. Coursework/Training: Graduate of an accredited school for medical assistants, or an equivalent combination of coursework and experience/training sufficient to qualify to sit for the Washington State Certification exam.
Research Associate The Evergreen State CollegeResearch AssociateOlympia, WAFull timeThe ideal candidate will have a background in policy analysis and a broad interest in evidence-based public policy; be a self-starter; be comfortable with ambiguity; possess strong quantitative, data analytical, communication, project management, and interpersonal skills; and have an eagerness to learn. A full state benefits package which includes: paid sick and vacation leave; paid campus holidays; a generous medical, dental, life and disability insurance package for employees and dependents; retirement; optional deferred compensation and optional supplemental retirement accounts.
Clinical Research Assistant - Lacey Providence Health & ServicesClinical Research Assistant - LaceyLacey, WARequsition ID: 429122 Company: Providence Jobs Job Category: Research Job Function: Clinical Support Job Schedule: Part time Job Shift: Day Career Track: Clinical Support Department: 3033 WA PCH MEDICAL RESEARCH PROJECTS Address: WA Lacey 4525 Third Ave SE Work Location: PRCS Lacey-Lacey Workplace Type: On-site Pay Range: $22.44 - $34.33 Responsibilities include coordinating study timelines and resources, ensuring accurate collection and submission of research data to sponsors, and supporting regulatory compliance through informed consent preparation, regulatory documentation, adverse event and protocol deviation reporting, and continuing review activities.
Clinical 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.
Clinical 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.
Senior Medical Director, Clinical Research Neurology Sumitomo PharmaSenior Medical Director, Clinical Research NeurologyOlympia, WA$284,320–$355,400 / yearSumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. **Our** **Mission** _To broadly contribute to society through value creation based on innovative research and development activities for the betterment of healthcare and fuller lives of people_ _worldwide_ **Our** **Vision** _For Longer and Healthier Lives, we unlock the future with cutting edge technology and_ _ideas_
Research Fellow, Medical Device Toxicologist Bausch + LombResearch Fellow, Medical Device ToxicologistOlympia, WA$150,000–$200,000 / yearThe Research Fellow - Medical Device Toxicologist will provide cross functional Preclinical medical device expertise supporting internal and external stakeholders pertaining to biocompatibility and associated focus areas, for medical device development, product expansion and maintenance. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe.
Research Scientist (Temporary), RGUD University of WashingtonResearch Scientist (Temporary), RGUDOlympia, WAThe Reproductive, Genitourinary and Digestive (RGUD) disease estimation team maintains and advances quantitative understanding of the health impacts, levels and trends of digestive diseases (including liver conditions - cirrhosis, hepatitis, and non-alcoholic fatty liver disease), gynecological and urinary disorders, sexually transmitted infections, and maternal disorders, and a subset of endocrine, metabolic, blood and immune disorders. **Job Description** **The Institute for Health Metrics and Evaluation (IHME) has an outstanding opportunity for a Research Scientist to join their Reproductive, Genitourinary and Digestive (RGUD) disease estimation team.** **About this Opportunity** Reporting to the Acting Assistant Professor, the Research Scientist is responsible for driving high-impact global health research at IHME, analyzing quantitative data across causes of death, epidemiology, and social determinants to produce key estimates that inform global health policy.
Research Fellow, Pharma Toxicology Bausch + LombResearch Fellow, Pharma ToxicologyOlympia, WA$150,000–$200,000 / yearThe Research Fellow, Pharma Toxicology, will provide comprehensive, cross functional preclinical expertise to internal and external stakeholders, with a focus on toxicology, and related scientific disciplines that support pharmaceutical development, and ongoing lifecycle management. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe.
Institutional Research Analyst Centralia CollegeInstitutional Research AnalystCentralia, WARespond to on-going and ad-hoc data requests from administrators, faculty, staff, and the public by producing tables, graphs, and narrative analysis of student characteristics, enrollment, retention, graduation, transfer, post-college employment, etc. Pursuant to RCW 28B.112.080, applicants must declare whether they are the subject of any substantiated findings of sexual misconduct in any current or former employment or is currently being investigated for, or have left a position during an investigation into, a violation of any sexual misconduct policy at the applicants current or past employers.
Staff Counsel or Research Analyst Washington State Senate Committee ServicesStaff Counsel or Research AnalystOlympia, WAThe Senate offers a comprehensive benefits package including medical, dental, vision, life and long-term disability insurance; vacation, sick, military, bereavement, and civil leave; twelve paid holidays per year; a state retirement plan; deferred compensation; healthcare flexible spending account; dependent care assistance; infant at work policy, optional credit unions; paid subscription to DeleteMe; and tuition reimbursement. · Ability to effectively interact and promote trust with others who have diverse racial and ethnic backgrounds, religious views, cultural backgrounds, socio-economic statuses, gender identities, sexual orientations, veteran statuses, geographical backgrounds, educational backgrounds, and disability statuses.
Research Principal, Real World Evidence CytelResearch Principal, Real World EvidenceOlympia, WASubject matter expertise in causal inference methods for comparative effectiveness studies, including target trial emulation, and/or developing real-world external control arms for clinical trials + Extensive experience with large healthcare real-world databases (electronic health records, claims databases) + Strong programming in R + Experience, vision, creativity, scope, integrity, leadership skills, prestige and intellect to enhance the existing organization and constructively contribute to the strategic direction of Cytel. Responsible for junior staff meeting the technical aspects their career development goals + Leadership or significant contributions to scientific processes involved with client deliverables (e.g., report templates, analysis plans, development of internal software/tools) + Can identify independently relevant methods, techniques and evaluation criteria for obtaining results + Keep abreast with regulatory, reimbursement and other industry requirements and guidelines, including via active participation in scientific conferences and symposia.
Principal Application Security Engineer - Threat Research CVS HealthPrincipal Application Security Engineer - Threat ResearchOlympia, WA$144,200–$288,400 / yearEducation** + Bachelor's degree or equivalent experience (High School Diploma and 4 years relevant experience) **Pay Range** The typical pay range for this role is: $144,200.00 - $288,400.00 This pay range represents the base hourly rate or base annual full-time salary for all positions in the job grade within which this position falls. **Position Summary** As the Principal Application Security Engineer - Threat Research, you will sit at the forefront of securing modern healthcare technology, combining deep engineering expertise with advanced threat research to protect applications and sensitive data at scale.
Spanish Bilingual Registered Dietician Clinical Trials Telehealth - Per Diem - Washington IQVIASpanish Bilingual Registered Dietician Clinical Trials Telehealth - Per Diem - WashingtonOlympia, WARemoteKey Responsibilities** As a Remote Registered Dietitian, you will: + Conduct nutritional assessments via telehealth and develop individualized dietetic care plans for patients with varying disease classifications + Provide ongoing dietary counseling and education to patients and their families + Deliver nutrition services **only to patients in states where you are licensed to practice** + Support patients enrolled in clinical research studies by monitoring nutritional progress and adherence + Maintain accurate, timely, and confidential clinical documentation + Participate in virtual team meetings, training sessions, and study-related activities **Qualifications** + Credentialed **Registered Dietitian (CDR)** with current national registration + Active, unrestricted **state licensure** (except CA, MI, NJ, AZ, VA, and CO) + Minimum **1 year of experience** providing nutrition planning and patient coaching + Minimum **1 year of experience delivering care remotely** via telehealth + Strong communication and interpersonal skills + Experience working with patients with obesity, with or without diabetes (preferred) + Experience managing patients on **GLP-1 therapies** (preferred) + **Spanish-English bilingual proficiency is required.** **Why Join IQVIA?** + Flexible per diem schedule that fits your lifestyle + Opportunity to gain exposure to clinical trials and research-focused care + Competitive supplemental income + Be part of a global organization advancing innovation and patient outcomes **Additional Information** + This position is **not eligible for visa sponsorship** . \#LI-CES and #LI-DNP #LI-HCP #remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
Mgr Medical Affairs - Clinical Scientist Canon USA & AffiliatesMgr Medical Affairs - Clinical ScientistOlympia, WA$112,000–$203,000 / yearClinical Research and Validation** + Manage collaborative research and clinical evaluation projects at collaboration/partner sites including data collection, protocol development, data acquisition, phantom studies, equipment evaluations, post processing, co-writing papers, IP and technology transfer support, and development of presentations. **Mgr Medical Affairs - Clinical Scientist - req1715** **OVERVIEW** Work as part of a dynamic and fast-paced team of clinical and technical experts dedicated to positively impacting clinical care by effectively translating innovative imaging solutions to the clinical environment.
Leader Medical Affairs Canon USA & AffiliatesLeader Medical AffairsOlympia, WA10 years' experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting or 3 years of experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting plus 7 years of experience in healthcare industry as imaging scientist or research manager. **Leader Medical Affairs - req1704** **OVERVIEW** Lead a team of clinical and technical experts dedicated to positively impacting clinical care by effectively translating innovative imaging solutions to the clinical environment.
Director, Global Clinical Development Otsuka America Pharmaceutical Inc.Director, Global Clinical DevelopmentOlympia, WAResponsibilities** : Otsuka is seeking an Associate Director/Director/Senior Director, Global Clinical Development based in our Rockville, MD or Princeton, NJ offices, who will be responsible for the design and oversight of clinical research programs and protocols for OPDC products under good clinical practices (GCP). + Its goal is to efficiently evaluate the product's potential and probability of success, support an effective commercial launch and plan for meaningful innovations to improve or expand the value of the initial product for our global customers (patients, prescribers and payors).