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.
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.
Senior Clinical Research Associate/Clinical Research Associate - All US Locations - FSP ParexelSenior Clinical Research Associate/Clinical Research Associate - All US Locations - FSPOlympia, WAFollows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance issues to Local Management and/or Clinical Quality Management (CQM) as required. The CRA is responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies, in compliance with Client Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies.
Clinical Research Associate/Senior Clinical Research Associate- FSP ParexelClinical Research Associate/Senior Clinical Research Associate- FSPOlympia, WAFollows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance issues to Local Management and/or Clinical Quality Management (CQM) as required. The CRA is responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies, in compliance with Client Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies.
NewSenior Clinical Research Coordinator Gastro HealthSenior Clinical Research CoordinatorOlympia, WA$65,000–$90,000When you join Gastro Health, you become part of a team dedicated to supporting clinical research and discovering new treatments for diseases, as well as new ways to detect, diagnose, and reduce the chance of developing diseases. Work closely with the PI to ensure compliance with protocols, and successfully conduct all assigned study-related activities in accordance with FDA and ICH GCP guidelines.
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.
Research Coordinator 1 - General Internal Medicine (Temporary) University of WashingtonResearch Coordinator 1 - General Internal Medicine (Temporary)Olympia, WAThe Research Coordinator's responsibility will involve traveling to prisons in western Washington to enroll participants in a study about alcohol and substance use, screening potential participants for enrollment, completing consent processes with potential participants, and administering the data collection tool, which includes a portion that is interviewer-administered. Approximately 80% of job responsibilities (up to 4 days/week) will be spent collecting data at prisons in Shelton, Washington (approximately 2/3 of data collection days) and Gig Harbor, Washington (approximately 1/3 of data collection days) in-person.
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, WARemoteThe 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. Experience in working with large data sets, including devising strategies for reliable data management for large data sets, computationally efficient modeling techniques to use such data sets, and critical evaluation of highly multidimensional model outputs that result from such work.
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 IQVIA Holdings IncSpanish Bilingual Registered Dietician Clinical Trials Telehealth - Per Diem - WashingtonOlympia, WARemoteThe potential base pay range for this role is The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). 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).