Research associate jobs in Tigard, OR - 318 jobs

Reality Labs at Meta is seeking Research Scientists with experience in product-focused machine learning and signal processing research to advance our pioneering work in neuromotor interfaces, which has grown out of the acquisition of CTRL-labs. We're building a practical interface drawing on the rich neuromotor signals that can be measured non-invasively via surface electromyography (EMG) with single motor neuron resolution. This technology could become one of the main pillars for interaction with virtual and augmented worlds.We are a multi-disciplinary team of researchers investigating the nature of human neuromotor signals, developing novel signal processing and machine learning methods to infer a user's intent, and creating novel interaction techniques and user experiences. Help us unleash human potential by removing the bottlenecks between user intent and action. **Required Skills:** Research Scientist - CTRL Labs Responsibilities: 1. Research and develop Deep Learning or other computational models 2. Design methods, tools and infrastructure to analyze and leverage rich multimodal data sets 3. Set technical direction for a project of 2-3 researchers and engineers 4. Help transition and deliver our work from research into product 5. Adapt standard machine learning methods to best leverage modern parallel environments (e.g. distributed clusters, multicore SMP, and GPU) **Minimum Qualifications:** Minimum Qualifications: 6. Bachelor's degree in Computer Science, Computer Engineering, relevant technical field, or equivalent practical experience 7. Ph.D. degree in Computer Science and Engineering, Electrical Engineering, Statistics/Mathematics 8. Experience with developing machine learning models at scale from inception to business impact 9. Programming experience in Python and hands-on experience with frameworks such as PyTorch 10. Exposure to architectural patterns of large scale software applications 11. Must obtain work authorization in the country of employment at the time of hire, and maintain ongoing work authorization during employment **Preferred Qualifications:** Preferred Qualifications: 12. Proven track record of achieving significant results as demonstrated by grants, fellowships, patents, as well as first-authored publications at peer-reviewed AI conferences (e.g. NeurIPS, CVPR, ICML, ICLR, ICCV, ACL, and ICASSP) 13. Demonstrated software engineer experience via an internship, work experience, coding competitions, or widely used contributions in open source repositories (e.g. GitHub) 14. Experience bringing machine learning-based products from research to production **Public Compensation:** $184,000/year to $257,000/year + benefits **Industry:** Internet **Equal Opportunity:** Meta is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state and local law. Meta participates in the E-Verify program in certain locations, as required by law. Please note that Meta may leverage artificial intelligence and machine learning technologies in connection with applications for employment. Meta is committed to providing reasonable accommodations for candidates with disabilities in our recruiting process. If you need any assistance or accommodations due to a disability, please let us know at accommodations-ext@meta.com.

Job Title: Research Associate Reports To: Dr. Marissa Kellogg Job Status: Limited Duration, Part Time, Non-Exempt Pay Rate: $30.00-45.00 per hour DOE A parttime (2-15 hours per week) Research Data Analyst - ideally someone trained/experienced in statistical genetics and/or computational biology/neuroscience - is being recruited for a VA Portland Healthcare System (VAPORHCS)-based research team that examines the genetics, genomics, and genetic epidemiology of neurological disease (i.e., epilepsy, stroke and traumatic brain injury) using data from the VA's Million Veteran Program (MVP) genetic research database. The incumbent will possess independent problem-solving skills, a high level of reliability and self-motivation, established organizational skills (including genetic database searching and data management), computer coding experience (e.g. Python, R, SQL, PLINK) excellent interpersonal communication skills, and the ability to work in a complex and multidisciplinary national research team. ESSENTIAL DUTIES AND RESPONSIBILITIES Perform phenotyping analysis of healthcare data from adults with epilepsy, stroke, traumatic brain injury (TBI) including deep clinical phenotyping of individuals based on electronic health record (EHR) and survey data using Human Phenotype Ontology (HPO) terminology and NIH's Common Data Elements (CDEs); statistical/computational phenotyping via utilization and validation of healthcare administrative algorithms and machine-learning models; and systematic databasing of phenotypic data. Perform genetic/genomic analysis of genotyping data (i.e. microarray and whole genome sequencing [WGS] results) from adults with epilepsy, stroke, TBI including: analyzing genetic information to determine the risk levels for specific genetic conditions; genotype-phenotype correlations; determining if genetic variants could be responsible for phenotypes via genetic database-based research (e.g., ClinVar, OMIM, Varisome, etc.); and systematically databasing genetic data. Recordkeeping, data organization and data management (e.g., study records, data entry into databases, data checking and cleaning, data harmonization, data summary, data analysis, and data graphing) on secure virtual platforms behind the VA firewall. Study team member responsibilities: regular research team meeting attendance; dissemination of study results in the form of writing/editing/preparing abstracts, posters, and manuscripts; writing grant applications; and participation in conferences and professional associations to upgrade skills and learn about new developments in genetics, genomics, and genetic epidemiology. JOB DUTIES Technical duties (specific to those listed above) include phenotype-genotype correlation studies, electronic health record-based research methods, genetic database searching and management, statistical and/or bioinformatic analysis techniques, applying machine-learning algorithms to healthcare data, and a clinical understanding of neurological disease and gene-environment interactions. QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. EDUCATION Completion of a master's degree (or higher doctoral degree) with major courses in relevant field of study: genetic counseling, genetics (clinical, statistical or quantitative), molecular and cellular biology, computational biology, neuroscience, computer science, bioinformatics, statistics, epidemiology, public health, or a related scientific discipline. College-level or above math or statistics is required. Graduate level statistics and/or computer coding coursework is preferred. Certification (or eligibility) with American Board of Genetic Counseling (ABGC) or American Board of Medical Genetics and Genomics (ABMGG) is preferred. EXPERIENCE Must have prior experience with scientific writing, as evidenced by authorship on peer-reviewed publications. Prior research experience in genetics, genomics, clinical research, neuroscience, neurology, computational biology, biostatistics, bioinformatics, public health, or epidemiology, is preferred. Experience with Microsoft office, genetic database search capability (i.e., ClinVar, OMIM, Varisome, Annovar, etc.), and database management (i.e., REDCap, MS Access, or SQL-based databases) is required. Experience with statistical and/or database-relevant coding (i.e., R, SQL, PLINK, command line, and/or Python) is preferred. SKILLS & ABILITIES Ability to communicate effectively with the research team in English is required. ADDITIONAL INFORMATION Because this position is based in a VA facility, the successful candidate must secure a VA Without Compensation Appointment (WOC) prior to starting work, and must maintain a WOC Appointment in order to continue employment. The VA's WOC process will be facilitated by the supervisor and processed through the VA Research and Development office. The screening process required to obtain a WOC may include a background check, a credit check, a physical, a drug test, and a TB test. After the WOC process has been completed, the VA also requires several trainings prior to employees starting work. Portland VA Research Foundation is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to status as a protected veteran or a qualified individual with a disability, or other protected status such as race, color, sex, sexual orientation, gender identity, religion, national origin or age. Portland VA Research Foundation uses E-Verify to confirm the identity and employment eligibility of all new hires. All PVARF employees are required to be fully vaccinated for COVID-19 within 8 weeks of hire, unless medically exempt. Employees will be required to provide either proof of vaccination or an approved medical exemption prior to beginning work. Because this position is based in a VA facility, the Research Associate must secure a VA Without Compensation Appointment (WOC) prior to starting work, and must maintain a WOC Appointment in order to continue employment. The VA's WOC process will be facilitated by the supervisor and processed through the VA Research and Development office. The screening process required to obtain a WOC can include a background check, a credit check, a physical, and a TB test.

The Johnson lab within the department of Molecular Microbiology & Immunology (MMI) focuses on two human herpes viruses: herpes simplex virus (HSV) and human cytomegalovirus (HCMV). The lab studies interactions between these viruses and host cells, the immune system, and viral pathogenesis. This position will assist in the investigation of how human cytomegalovirus infects and spreads in relevant human cell types with the focus on characterizing virus membrane glycoprotein function and interactions with host cell receptor molecules. The position will also involve performing virology based assays using a variety of mammalian cell lines in a tissue culture model system. Additional duties will include characterizing virus and host cell proteins by western blot, ELISA assays, immunofluorescent microscopy and other standard techniques. This position will also entail performing additional molecular biology techniques such as recombinant DNA technology, protein expression and purification, antibody production, and preparation of live viruses. Some lab management duties such as administration of IACUC protocols, general lab maintenance, ordering, and reagent preparation will also be required. Function/Duties of Position * Work independently to plan and execute experimental procedures to produce publication quality data for grants and manuscripts. * Preparation of detailed experimental reports including data analysis and image processing. * Assist in the general lab operations and maintenance of lab equipment. * Other duties as requested. Required Qualifications * Master's Degree in relevant field AND 3 years of relevant experience; OR * Bachelor's Degree in relevant field AND 5 years of relevant experience. Preferred Qualifications * Past experience with tissue culture, DNA cloning, and microscopy. Additional Details Work hours are Monday - Friday, 8:00am - 5:00pm, occasional weekends and evenings as needed. Work is performed in a laboratory setting that includes handling of infectious agents including viruses, hazardous chemicals and human samples. All are welcome Oregon Health & Science University values a diverse and culturally competent workforce. We are proud of our commitment to being an equal opportunity, affirmative action organization that does not discriminate against applicants on the basis of any protected class status, including disability status and protected veteran status. Individuals with diverse backgrounds and those who promote diversity and a culture of inclusion are encouraged to apply. To request reasonable accommodation contact the Affirmative Action and Equal Opportunity Department at ************ or *************.

The Johnson lab within the department of Molecular Microbiology & Immunology (MMI) focuses on two human herpes viruses: herpes simplex virus (HSV) and human cytomegalovirus (HCMV). The lab studies interactions between these viruses and host cells, the immune system, and viral pathogenesis. This position will assist in the investigation of how human cytomegalovirus infects and spreads in relevant human cell types with the focus on characterizing virus membrane glycoprotein function and interactions with host cell receptor molecules. The position will also involve performing virology based assays using a variety of mammalian cell lines in a tissue culture model system. Additional duties will include characterizing virus and host cell proteins by western blot, ELISA assays, immunofluorescent microscopy and other standard techniques. This position will also entail performing additional molecular biology techniques such as recombinant DNA technology, protein expression and purification, antibody production, and preparation of live viruses. Some lab management duties such as administration of IACUC protocols, general lab maintenance, ordering, and reagent preparation will also be required. Function/Duties of Position Work independently to plan and execute experimental procedures to produce publication quality data for grants and manuscripts. Preparation of detailed experimental reports including data analysis and image processing. Assist in the general lab operations and maintenance of lab equipment. Other duties as requested. Required Qualifications Master's Degree in relevant field AND 3 years of relevant experience; OR Bachelor's Degree in relevant field AND 5 years of relevant experience. Preferred Qualifications Past experience with tissue culture, DNA cloning, and microscopy. Additional Details Work hours are Monday - Friday, 8:00am - 5:00pm, occasional weekends and evenings as needed. Work is performed in a laboratory setting that includes handling of infectious agents including viruses, hazardous chemicals and human samples. All are welcome Oregon Health & Science University values a diverse and culturally competent workforce. We are proud of our commitment to being an equal opportunity, affirmative action organization that does not discriminate against applicants on the basis of any protected class status, including disability status and protected veteran status. Individuals with diverse backgrounds and those who promote diversity and a culture of inclusion are encouraged to apply. To request reasonable accommodation contact the Affirmative Action and Equal Opportunity Department at ************ or *************.

Department: DSGN Planning, Public Policy and Management Rank: Research Assistant (Type C), Research Associate Annual Basis: 12 Month Review of Applications Begins September 16, 2024, applications reviewed as needs arise Special Instructions to Applicants To ensure consideration, please include the following with your online application: • Current resume which outlines your educational and professional work experience, including dates of employment. • Name and contact information for three professional references. Candidates will be notified prior to references being contacted. Any application missing the above information may be considered incomplete. Department Summary The Sustainable Cities Institute (SCI) is an applied think tank focusing on sustainability in cities. We work across disciplines inside and out of academia to redefine the delivery of higher education, conduct applied and policy-relevant research, and serve the public in the design and development of sustainable, resilient, and livable cities. Our work is consistently applied, multi-disciplinary, and sustainability-focused, matching the complexity of cities with the disciplinary expertise to match. We focus on everything in cities, from sustainable architecture to transportation to engaging marginalized communities to impacting the larger, relevant policy frameworks at the local and state levels. The Urbanism Next Center at the University of Oregon conducts research and convenes partners from around the world to understand the impacts of new mobility, urban delivery, and autonomous vehicles on the built environment. Going beyond these emerging technologies, we explore the possible implications on equity, health and safety, the economy, and the environment to inform decision-making that supports community goals. Urbanism Next brings together experts from a wide range of disciplines including planning, design, development, business, and law and works with the public, private, and academic sectors to help create positive outcomes from the impending changes and challenges confronting our cities. Urbanism Next is a rapidly evolving and changing organization with an entrepreneurial spirit and will offer opportunities for change and growth to research staff. Position Summary The University of Oregon's Urbanism Next Center seeks to create a pool of qualified candidates to fill periodic vacancies for pro-tem research/project management positions. All positions would be funding contingent, temporary assignments with an appointment of up to one year, but with the possibility of renewal for up to a total of three years depending on need, funding, and/or performance. Appointments would be as research assistants or associates, conducting research or project management under the direction of a principal investigator. We invite applications from qualified candidates who share our commitment to diversity and from members of underrepresented groups. Minimum Requirements To qualify for the rank of Research Assistant (Type C): • Master's in Planning, Public Administration, Environmental Studies, or a related field. In exceptional circumstances, a Bachelor's degree and significant professional experience in a relevant field may substitute. • Experience with applied research. To qualify for the rank of Research Associate: • Ph.D. in Planning, Public Administration, Environmental Studies, or a related field. • Experience with applied research. Professional Competencies • Professional experience in applied research and ability to work with other faculty, staff, and clients at the University of Oregon. All offers of employment are contingent upon successful completion of a background check. The University of Oregon is proud to offer a robust benefits package to eligible employees, including health insurance, retirement plans, and paid time off. For more information about benefits, visit ************************************** The University of Oregon is an equal opportunity, affirmative action institution committed to cultural diversity and compliance with the ADA. The University encourages all qualified individuals to apply and does not discriminate on the basis of any protected status, including veteran and disability status. The University is committed to providing reasonable accommodations to applicants and employees with disabilities. To request an accommodation in connection with the application process, please contact us at ********************* or ************. UO prohibits discrimination on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, gender expression, pregnancy (including pregnancy-related conditions), age, physical or mental disability, genetic information (including family medical history), ancestry, familial status, citizenship, service in the uniformed services (as defined in federal and state law), veteran status, expunged juvenile record, and/or the use of leave protected by state or federal law in all programs, activities and employment practices as required by Title IX, other applicable laws, and policies. Retaliation is prohibited by UO policy. Questions may be referred to the Office of Investigations and Civil Rights Compliance. Contact information, related policies, and complaint procedures are listed here. In compliance with federal law, the University of Oregon prepares an annual report on campus security and fire safety programs and services. The Annual Campus Security and Fire Safety Report is available online at ************************************************************************

Occasional part-time hourly work with hours ranging from 0-25 hours per week depending on availability of assignments. Work consists of music and market research in businesses in various states. Assignments include onsite research in businesses during late evenings, including weekends. Assignments also require completion of detailed reports following on-site visits. FUNCTIONS OF THE JOB: Conduct in-person research in businesses as assigned. Complete detailed reports of music used in a business during in-person research. Recording of music performance(s). Photographing both exterior and interior of locations. POSITION QUALIFICATION REQUIREMENTS Must be 21+ years of age. Able to conduct on-site research in businesses during late evenings and weekends. Strong interpersonal skills. Good communication skills, both written and oral. Proficient in basic computer skills. Strong time management and organizational skills. Detail oriented. This job description in no way states or implies that these are the only duties to be performed by the employee occupying the position. Employees may be required to follow other job-related instructions and perform other job-related duties as requested, subject to all applicable state and federal laws. “Commonly associated” is not intended to mean always or only. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Innovative research paves the way for improved patient outcomes. You can be a part of the research that's driving new treatments and procedures at Legacy. In your role, you will provide clinical or scientific expertise to a team working to transform medical care. If you're ready to grow your skills and share in the Legacy mission of making life better for others, we invite you to consider this opportunity. A Postdoctoral Research Fellow position is available at Legacy Devers Eye Institute, Portland, Oregon. The successful candidate will be responsible for carrying out independent research, working closely with Dr. Kazuhiro Kurokawa and his team at Discoveries in Sight Research Laboratories. A unique and specialized research environment will allow you to address key scientific questions requiring accurate and precise measurements. Specifically, we will leverage the full potential of adaptive optics optical coherence tomography (AO-OCT) and fluorescence scanning laser ophthalmoscope (AO-fSLO) to study glaucoma and other neurodegenerative diseases. We encourage you to apply if you want to make a difference. We are looking for a Postdoctoral Research Fellow with relevant background in the fields of biomedical engineering, ophthalmic imaging, vision science, and ophthalmology. Since the study involves both software and hardware design, development, and delicate implementation, the Postdoctoral Research Fellow is expected to have a strong engineering background as well, especially in the field of computer science and optics. Also, it is critical to have excellent communication skills to work with other colleagues with diverse backgrounds. The ideal candidate will be self-motivated, pay close attention to the details and their environment, and eager to learn basic, translational, and clinical research as well as new imaging technologies. Legacy Devers Eye Institute - Discoveries in Sight: Discoveries in Sight is a private, nonprofit research institute - one of only a handful in the United States that is focused on the visual system. Visiting clinicians, scientists, medical students, and postdoctoral fellows come from around the world (including England, France, Belgium, Brazil, Korea, Singapore, Japan, Switzerland, Italy, China, Germany, Nepal and South Africa) in order to draw on our research expertise. Our goal is to expedite the development of new technologies and treatments to prevent, detect and treat blinding eye disease through programs that include: Basic Research: Combining novel research programs in ocular anatomy, physiology, and pharmacology to discover their roles in ocular and central visual system disease. Clinical Research: Initiating and conducting clinical trials to test new diagnostic instruments and therapies. Clinical Epidemiology: Prevalence of eye disease in populations Technology Development: Working with industry to accelerate the development of new technologies and pharmaceuticals. All interested and qualified candidates are encouraged apply. Responsibilities A Post-Doctoral Research Fellow is an MD or Ph.D. in a scientific discipline. Post-Doctoral Research Fellows may provide clinical and/or scientific services, according to their level of responsibility, under the supervision of the Principal Investigator with the common goal of accelerating the development of new technologies and treatments in assigned area. Qualifications Education: MD or Ph.D. in a scientific discipline. At a minimum the individual must have documentation they have completed all of the course work, research, and thesis preparation and acceptance necessary to receive their degree. This recognizes that granting institutions (universities) only present degrees on a periodic schedule. Skills: Excellent communication, organizational and time management skills. Ability to work independently. Pay Range USD $32.56 - USD $44.75 /Hr. Our Commitment to Health and Equal Opportunity Our Legacy is good for health for Our People, Our Patients, Our Communities, Our World. Above all, we will do the right thing. If you are passionate about our mission and believe you can contribute to our team, we encourage you to apply-even if you don't meet every qualification listed. We are committed to fostering an inclusive environment where everyone can grow and succeed. Legacy Health is an equal opportunity employer and prohibits unlawful discrimination and harassment of any type and affords equal employment opportunities to employees and applicants without regard to race, color, religion or creed, citizenship status, sex, sexual orientation, gender identity, pregnancy, age, national origin, disability status, genetic information, veteran status, or any other characteristic protected by law. To learn more about our employee benefits click here: ********************************************************************

Job Description Practice/Department: Emerging Regions Internal Title: As-Needed Biologist Work Environment: Field with up to 20% office work Compensation: $25-35/hourly * Dudek's journey began in 1980 with a vision to serve Southern California's water and wastewater agencies. Today, we are a 100% employee-owned firm supporting clients nationwide and delivering projects that improve and protect the built and natural environments of communities throughout the United States. Our work has been recognized by leading industry organizations, and we've been honored with multiple national Top Workplace Awards. Our employee-owners are unified by a singular commitment to supporting projects that address key societal issues, such as the transition to renewable energy, infrastructure hardening and repair, environmental protection, and community resilience. Learn more about our award-winning culture, the benefits and perks of being a Dudekian, and the projects you will have the opportunity to shape. Who You Are As an employee-owner, you embrace accountability, working safely, and collaboration while thinking resourcefully and independently. Like all Dudekians, you are curious and solution-oriented, with the ability to adapt quickly to changes and approach challenges with a spirit of innovation. How You'll Make an Impact Dudek is seeking field biologists and botanists to provide as-needed field support for projects in Oregon and Washington. This position will provide biologists with 2-6+ years of of experience to support a variety of projects in the Pacific Northwest, including projects related to utility infrastructure upgrades and renewable energy generation and storage. Strong candidates will have extensive outdoor experience, particularly through agencies, volunteering, or graduate schoolwork. Candidates with strong writing skills and a desire to assist with reporting will be given the chance to do so. Duties and Responsibilities Conduct site assessments, surveys, and habitat evaluations for common and special-status plant and wildlife species and map vegetation communities Conduct wetland delineations pursuant to federal and state requirements Record and take notes on a mobile device Follow all Dudek and project site safety protocols Hike long distances in potentially inclement weather, heat, and rough terrain Apply a high level of attention to detail and work independently and as a part of a team Minimum Qualifications Bachelor's degree in biology, environmental science, or other related field; OR a minimum of 1-3 years demonstrated field experience in biological resource management and surveying Knowledge of and ability to identify Oregon and Washington wildlife and/or plant species Must possess a valid driver's license and have active personal automobile liability insurance by the first day of employment Preferred Qualifications 2-6+ years of experience in environmental field settings in Oregon and Washington Understanding of and familiarity with environmental regulations and permits Strong botanical knowledge including experience identifying common and rare plant species and/or using dichotomous keys to identify Pacific Northwest plants. Experience executing species-specific survey protocols, e.g., marbled murrelet, western toad, northern spotted owl, northwestern pond turtle. 4-wheel-drive experience Professional Wetland Scientists (PWS) or Wetland Professionals in Training (WPIT), are preferred. Compensation: $25-35/hourly* *Final agreed-upon compensation will be based on a variety of factors including, but not limited to, an individual's related experience, education, certifications, skills, and work location. Successful candidates must pass a pre-employment drug test and background check prior to beginning employment. Working Conditions: Environment This job operates in a remote or office-based environment and this role routinely uses standard office equipment such as computers, phones, printers, etc. This job may also require occasional project site visits, based outdoors which can include excessive noise, uneven walking surfaces, extreme weather, and moving vehicles and equipment. Physical Requirements The physical demands described here are representative of those that must be met to successfully perform the essential functions of the job. This job requires the following: Working on a computer, sitting, or standing for long periods of time in an office or remote office setting. Employees must be capable of bending, squatting, climbing ladders, and lifting up to 35 lbs. unassisted; 50lbs in a team lift (two or more employees). Attending meetings, both in person and virtually, and speaking on the phone with peers, clients, etc. Specific vision abilities, including close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus. Dudek is committed to creating a workplace where all employees, regardless of their background, feel valued, respected, and have equal opportunities to succeed. We believe that a diverse and inclusive workforce is essential to our business success, and we are dedicated to fostering a culture where everyone can thrive. We are committed to fair and equitable processes, based on merit, free from any discrimination. Dudek is genuinely committed to equal employment opportunities within our company and on our project teams. Dudek is also committed to compliance with all applicable laws providing equal employment opportunities. This commitment applies to all persons involved in Dudek's operations and prohibits unlawful discrimination by any employee of Dudek, including supervisors and coworkers. Equal employment opportunities will be extended to all persons (including those with disability and veteran status) in all aspects of the employment relationship, including recruitment, hiring, training, promotion, transfer, compensation, benefits, discipline, layoff, recall, and termination. Any employee who violates this policy and Dudek's commitment to equal employment opportunities will be subject to disciplinary action. Dudek is a U.S.-based employer. All positions are based in the United States and require U.S. work authorization Powered by JazzHR HVGIh82rKT

Senior Research Associate - Portland, OR (Onsite) ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We have an incredible opportunity for a Senior Research Associate to join ICON's Specialty Lab in Portland, Oregon, within the PCR Development Team. The Senior Research Associate is responsible for the completion of experiments and written assignments as directed by senior laboratory staff and management for the purpose of developing, optimizing, and validating molecular-based assays for implementation in clinical trial testing. Location: Portland, OR (100% onsite) Hours: Monday - Friday; 8:00am - 5:00pm What you will be doing: * Designing and implementing research studies to gather data and insights * Analyzing research data to identify trends, patterns, and areas for improvement * Collaborating with cross-functional teams to develop research methodologies and protocols * Preparing research reports and presentations to communicate findings to stakeholders * Ensuring data integrity and accuracy through rigorous validation processes * Staying updated on industry trends and emerging technologies to enhance research capabilities * Contributing to organizational growth through effective research and strategic planning Your profile: * 3+ years of laboratory bench experience, preferably in a regulated industry setting * PCR-based assay development and validation experience (Digital PCR experience preferred) * Strong proficiency in research methodologies and data analysis tools, with excellent attention to detail * Excellent analytical and problem-solving skills, with the ability to develop effective research strategies * Demonstrated ability to work collaboratively with cross-functional teams * Detail-oriented, with strong organizational skills to manage multiple projects and deadlines in a dynamic environment * Bachelors Degree in Life Sciences or a related field #LI-TP1 #LI-Office What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: * Various annual leave entitlements * A range of health insurance offerings to suit you and your family's needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. * Life assurance * Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Absci is a clinical-stage biotechnology company advancing novel therapeutics using generative AI. Our Integrated Drug Creation™ platform combines cutting-edge AI models with a synthetic biology data engine, enabling the rapid design of innovative therapeutics that address challenging therapeutic targets. Absci is a global company headquartered in Vancouver, WA, and maintains offices in New York City, Switzerland, and Serbia. Learn more at ************* or follow us on LinkedIn (@absci), X (@Abscibio), and YouTube. Senior Research Associate, Pharmacology & Bioassays Location: Vancouver, WA (Onsite) Position: Full-Time, Senior Research Associate (Sr. RA) We are seeking a highly motivated and skilled Senior Research Associate (Sr. RA) to join our Pharmacology & Bioassays team. The successful candidate will play a key role in advancing preclinical drug discovery by executing cell-based assays and cell line engineering for various therapeutic programs. This position involves hands-on benchwork and requires experience with primary cell culture, disease-relevant mechanistic assays, mechanisms of action (MoA) assays, and reporter cell-based assays. The role will focus on drug discovery, supporting mechanistic studies, and generating data to guide the progression of Absci's biologics pipeline. Key Responsibilities: Maintain and culture primary cell types, and run various in-vitro/ex-vivo assays contributing to the development of pharmacology work-packages. Contribute to design, development and hands-on execution of in-vitro and ex-vivo disease-relevant assays for MOA studies and therapeutic testing. Troubleshoot and refine assays, ensuring reproducibility and robustness in both medium- and high-throughput formats. Perform data analysis, interpret and present experimental data at various platforms. Collaborate with interdisciplinary teams, including cellular screening to integrate data from cell-based assays and support drug discovery goals. Contribute to the preparation of SOPs, study protocols, and data presentations for regulatory and internal purposes. Ensure adherence to best practices in assay development, data management, and experimental execution. Required Qualifications: BSc in Biology, Cell Biology, Immunology, Biotechnology, or related field with 5+ years of industry experience in cell-based assays and primary cell culture work, OR MSc with 3+ years of relevant industry experience. Hands-on experience in primary cell culture, including immune cells (PBMCs, T-cells, NK cells), cancer cell lines, and other disease-relevant models. Experience in mechanistic assays, such as MoA assays, ligand-binding assays, ADCC, CDC, ADCP, and cellular uptake assays. Experience in reporter cell-based assays, with the ability to develop and implement these assays. Experience with flow cytometry, ELISA, Western blot, qPCR, and multiplexing technologies. Proficiency in data analysis software such as GraphPad Prism, SoftMax Pro to interpret and visualize experimental results. Ability to troubleshoot assays, ensuring high-quality and reproducible data. Excellent communication skills, with the ability to present data effectively to a variety of stakeholders and contribute to decision-making. Strong organizational skills, with the ability to prioritize tasks and manage multiple projects simultaneously. Demonstrated success working in a matrixed, highly collaborative team environment, contributing to both individual and team goals. How We Thrive Together: Absci's Core Values We Believe in the Impossible We are one team with one finish line We embrace our differences We deliver Results We do the right thing Innovate because lives depend on it. Compensation and Benefits The salary range for this position is $88,000 - 100,000/year. The range provided is based on what we believe is a reasonable estimate for the base salary range for this job at the time of posting. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law Absci offers highly competitive salaries and benefits, including medical, dental, vision insurance, unlimited vacation, parental leave, employee assistance program, voluntary life and disability insurance, annual bonus potential, and 401(k) with a generous company match. Legal authorization to work in the United States is required. Absci is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, sexual orientation, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, marital status, or any characteristic protected under applicable law. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should request the recruiter or hiring manager or contact ****************.

The Dotter Department of Interventional Radiology serves as a beacon of both internationally recognized research and locally delivered advanced clinical care. The Dotter Department of Interventional Radiology is a part of the OHSU School of Medicine, with its own admitting service and clinic. We provide all the diagnostic angiographic, interventional radiologic, and neurointerventional services to the OHSU and VA Hospitals. The appointee shall provide services as assigned by the supervisor in furtherance of the university's missions and goals of teaching, research, patient care, outreach and public service. The individual hired for this position will serve as research faculty and lab manager for the Dotter Memorial Research Laboratory at the Dotter Institute. The role of the lab manager is to carry out and facilitate the educational and research projects at the Institute. This will be done under the supervision of the Director of Research, and the Director of the Institute overall. Activities include coordination of clinical and translational lab research, including protocol design, preparation and execution. The Dotter research lab offers additional educational workshops involving an animal model for which the lab manager is responsible to organize and conduct. We also support industry and academic collaborators by providing translational research support, device prototype testing, and running educational/teaching labs. The lab manager is expected to play an active role in reaching out to potential industry and academic collaborators to continue and expand our lab activities and scope. Coordination of maintenance requirements and updates of the research facility and interfacing with the Institutional Animal Care and Use Committee (IACUC) will also be administrative responsibilities of the position. Function/Duties of Position Coordinate clinical and translational lab research activities of the Dotter Institute Assist in providing education in translational procedures and in clinical training activities Assist in preparing lab publications, electronic media, and lectures Interface with industry and academic collaborators to facilitate clinical and translational projects Participate in funding applications to support research activities Provide mentorship and education to undergraduate, graduate and medical students, clinical residents, and clinical and research fellows for research activities of the Dotter Institute Oversight of the research facility including regulatory compliance, research personnel training and maintenance of lab equipment and inventory Required Qualifications Doctoral degree in relevant field and a minimum of 7 years of relevant post-doctoral work experience. Internal candidates must have completed 3-5 years at the Assistant Staff Scientist level. Familiarity with animal care and handling, anesthesia, animal surgery, pre- and post-procedural management Training and experience in scientific methods, including biostatistics and scientific protocol Familiarity with percutaneous procedures, equipment and devices Experience in teaching and mentorship All are welcome Oregon Health & Science University values a diverse and culturally competent workforce. We are proud of our commitment to being an equal opportunity, affirmative action organization that does not discriminate against applicants on the basis of any protected class status, including disability status and protected veteran status. Individuals with diverse backgrounds and those who promote diversity and a culture of inclusion are encouraged to apply. To request reasonable accommodation contact the Affirmative Action and Equal Opportunity Department at ************ or *************.

Senior Research Associate - Portland, OR (Onsite) ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We have an incredible opportunity for a Senior Research Associate to join ICON's Specialty Lab in Portland, Oregon, within the PCR Development Team. The Senior Research Associate is responsible for the completion of experiments and written assignments as directed by senior laboratory staff and management for the purpose of developing, optimizing, and validating molecular-based assays for implementation in clinical trial testing. Location: Portland, OR (100% onsite) Hours: Monday - Friday; 8:00am - 5:00pm What you will be doing: Designing and implementing research studies to gather data and insights Analyzing research data to identify trends, patterns, and areas for improvement Collaborating with cross-functional teams to develop research methodologies and protocols Preparing research reports and presentations to communicate findings to stakeholders Ensuring data integrity and accuracy through rigorous validation processes Staying updated on industry trends and emerging technologies to enhance research capabilities Contributing to organizational growth through effective research and strategic planning Your profile: 3+ years of laboratory bench experience, preferably in a regulated industry setting PCR-based assay development and validation experience (Digital PCR experience preferred) Strong proficiency in research methodologies and data analysis tools, with excellent attention to detail Excellent analytical and problem-solving skills, with the ability to develop effective research strategies Demonstrated ability to work collaboratively with cross-functional teams Detail-oriented, with strong organizational skills to manage multiple projects and deadlines in a dynamic environment Bachelors Degree in Life Sciences or a related field #LI-TP1 #LI-Office What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family's needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Senior Research Associate - Portland, OR (Onsite) ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We have an incredible opportunity for a Senior Research Associate to join ICON's Specialty Lab (****************************************************************************************************************** in Portland, Oregon, within the PCR Development Team. The Senior Research Associate is responsible for the completion of experiments and written assignments as directed by senior laboratory staff and management for the purpose of developing, optimizing, and validating molecular-based assays for implementation in clinical trial testing. **Location:** Portland, OR (100% onsite) **Hours:** Monday - Friday; 8:00am - 5:00pm **What you will be doing:** + Designing and implementing research studies to gather data and insights + Analyzing research data to identify trends, patterns, and areas for improvement + Collaborating with cross-functional teams to develop research methodologies and protocols + Preparing research reports and presentations to communicate findings to stakeholders + Ensuring data integrity and accuracy through rigorous validation processes + Staying updated on industry trends and emerging technologies to enhance research capabilities + Contributing to organizational growth through effective research and strategic planning **Your profile:** + 3+ years of laboratory bench experience, preferably in a regulated industry setting + PCR-based assay development and validation experience (Digital PCR experience preferred) + Strong proficiency in research methodologies and data analysis tools, with excellent attention to detail + Excellent analytical and problem-solving skills, with the ability to develop effective research strategies + Demonstrated ability to work collaboratively with cross-functional teams + Detail-oriented, with strong organizational skills to manage multiple projects and deadlines in a dynamic environment + Bachelors Degree in Life Sciences or a related field \#LI-TP1 \#LI-Office **What ICON can offer you:** Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: + Various annual leave entitlements + A range of health insurance offerings to suit you and your family's needs. + Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. + Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. + Life assurance + Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site (************************************* to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here (****************************************************** Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here (****************************************************** to apply

Senior Research Associate - Portland, OR (Onsite) ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We have an incredible opportunity for a Senior Research Associate to join ICON's Specialty Lab in Portland, Oregon, within the PCR Development Team. The Senior Research Associate is responsible for the completion of experiments and written assignments as directed by senior laboratory staff and management for the purpose of developing, optimizing, and validating molecular-based assays for implementation in clinical trial testing. Location: Portland, OR (100% onsite) Hours: Monday - Friday; 8:00am - 5:00pm What you will be doing: Designing and implementing research studies to gather data and insights Analyzing research data to identify trends, patterns, and areas for improvement Collaborating with cross-functional teams to develop research methodologies and protocols Preparing research reports and presentations to communicate findings to stakeholders Ensuring data integrity and accuracy through rigorous validation processes Staying updated on industry trends and emerging technologies to enhance research capabilities Contributing to organizational growth through effective research and strategic planning Your profile: 3+ years of laboratory bench experience, preferably in a regulated industry setting PCR-based assay development and validation experience (Digital PCR experience preferred) Strong proficiency in research methodologies and data analysis tools, with excellent attention to detail Excellent analytical and problem-solving skills, with the ability to develop effective research strategies Demonstrated ability to work collaboratively with cross-functional teams Detail-oriented, with strong organizational skills to manage multiple projects and deadlines in a dynamic environment Bachelors Degree in Life Sciences or a related field #LI-TP1 #LI-Office What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family's needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Site: The McLean Hospital Corporation Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham. Job Summary Summary Responsible for assisting clinical professionals in providing behavioral and mental health services to patients in a hospital setting. This position supports patient care through assessments, research, and administrative tasks under supervision, gaining foundational experience in social work and behavioral health. Does this position require Patient Care? Yes Essential Functions * Assist in patient assessments and collect relevant behavioral health information under supervision. * Support the implementation of therapeutic interventions, including individual and group counseling sessions. * Participate in clinical research projects, collecting and analyzing data related to patient outcomes and behavioral health trends. * Provide educational resources to patients and families on mental health, wellness strategies, and community support services. * Maintain accurate and confidential patient records, ensuring all documentation aligns with hospital and regulatory standards. * Collaborate with social workers, behavioral health professionals, and interdisciplinary teams to coordinate patient care and follow-up. * Assist in crisis intervention situations, providing support to stabilize patients under guidance. * Engage in ongoing training and professional development to enhance clinical knowledge and skills. Qualifications Education Bachelor's Degree Required Can this role accept experience in lieu of a degree? No Licenses and Credentials Experience Experience or internships in social work, mental health, or a related field 0-1 year preferred but not necessary Knowledge, Skills and Abilities * Strong verbal and written communication abilities to effectively interact with patients, families, and healthcare professionals. * Ability to provide empathetic care and support to patients dealing with behavioral and mental health challenges. * Capable of assisting in research, data collection, and analyzing patient information. * Strong organizational skills to manage documentation and patient interactions efficiently. * Ability to work effectively as part of a multidisciplinary team. * Flexibility in handling a variety of tasks in a dynamic and fast-paced clinical environment. It is the policy of McLean Hospital to affirmatively provide equal opportunity to all qualified applicants for employment and existing employees without regard to their race, religion, color, national origin, sex, age, ancestry, protected veteran status, disability, sexual orientation, gender identity or expression, pregnancy or a condition related to pregnancy including, but not limited to, lactation or the need to express breast milk for a nursing child, or any other basis that would be in violation of any applicable law or regulation. Additional Job Details (if applicable) Physical Requirements * Standing Frequently (34-66%) * Walking Frequently (34-66%) * Sitting Occasionally (3-33%) * Lifting Frequently (34-66%) * Carrying Frequently (34-66%) * Pushing Occasionally (3-33%) * Pulling Occasionally (3-33%) * Climbing Rarely (Less than 2%) * Balancing Frequently (34-66%) * Stooping Occasionally (3-33%) * Kneeling Occasionally (3-33%) * Crouching Occasionally (3-33%) * Crawling Rarely (Less than 2%) * Reaching Frequently (34-66%) * Gross Manipulation (Handling) Frequently (34-66%) * Fine Manipulation (Fingering) Frequently (34-66%) * Feeling Constantly (67-100%) * Foot Use Rarely (Less than 2%) * Vision - Far Constantly (67-100%) * Vision - Near Constantly (67-100%) * Talking Constantly (67-100%) * Hearing Constantly (67-100%) Remote Type Onsite Work Location 115 Mill Street Scheduled Weekly Hours 40 Employee Type Regular Work Shift Rotating (United States of America) Pay Range $22.88 - $32.72/Hourly Grade 5 At Mass General Brigham, we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive, and any offer extended will take into account your skills, relevant experience if applicable, education, certifications and other essential factors. The base pay information provided offers an estimate based on the minimum job qualifications; however, it does not encompass all elements contributing to your total compensation package. In addition to competitive base pay, we offer comprehensive benefits, career advancement opportunities, differentials, premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth. We invite you to apply, and our Talent Acquisition team will provide an overview of your potential compensation and benefits package. EEO Statement: The McLean Hospital Corporation is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran's Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact Human Resources at **************. Mass General Brigham Competency Framework At Mass General Brigham, our competency framework defines what effective leadership "looks like" by specifying which behaviors are most critical for successful performance at each job level. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance, make hiring decisions, identify development needs, mobilize employees across our system, and establish a strong talent pipeline.

The Division of Vascular Surgery at Oregon Health & Science University (OHSU) is offering clinical outcomes research fellowships to qualified candidates interested in an academic career in vascular surgery. Qualified candidates will benefit from extensive infrastructure and resources at OHSU Department of Surgery and the Knight Cardiovascular Institute. This includes established clinical databases, a Biostatistical core, and IT services. The successful clinical research fellow(s) will be integrated within the clinical surgical team to perform high-quality data analysis of relevant vascular surgical questions. This position will primarily work on vascular surgery projects with a special focus on peripheral artery disease, graft infections, vascular trauma, and vascular lab topics and other projects as assigned. This will include screening, consenting, and collecting data and biospecimens; entering or uploading data into the REDCap database; managing the database and updating it as needed; organizing and analyzing data for abstracts, presentations, and manuscripts. This person will assist with other papers, chapters, and grants when assigned. They will present at local and national scientific meetings. Successful candidates will have: Prior clinical vascular or general surgery training in the US, Canada, or internationally. Experience in Data abstraction Statistical analysis Manuscript preparation Demonstrated track record of academic productivity in presentation and peer-reviewed publications Applicants must be medical graduates with vascular or general surgery clinical training completed or in progress. Successful candidates would receive salary and benefits through OHSU. This is a 1 year position. Function/Duties of Position Clinical Research Coordination: screen, consent, collect data, and complete study visits as outlined in study protocols Data analysis: be able to complete basic analysis of data; be able to convey statistical needs to team; work with department biostatistician on more complex analysis; Database Management: build and maintain REDCap databases; abstract data from electronic medical record; upload data provided by system application analyst Writing: write and submit abstracts to scientific meetings; present data at meetings; organize and write manuscripts and chapters Grant applications: work with faculty to submit grants, includes writing, organizing, and submitting to department GCA required forms and documents Support OHSU Research Regulation & Policies Compliance Other Research Related Tasks Assigned: assisting with other department and division research activities when needed Required Qualifications Doctorate Degree in relevant field; Experience in data abstraction from electronic health records Basic statistical analysis and use of software programs such as SPSS, R, SAS, or STATA Self-starter with strong organizational skills and ability to prioritize work demands Excellent oral and written communication skills Meticulous detail to data and study procedures Ability to prioritize work demands and trouble shoot Ability to work independently in a multi-task collaborative environment Proficient knowledge of MS Word, MS PowerPoint, and MS Excel Preferred Qualifications Experience with large databases such as SVS and VQI IRB submissions Epic Database building and management in REDCap Additional Details This position is a Monday - Friday position with a hybrid (office, clinic, home) work schedule. It will primarily be an 8:00 am - 5:00 pm position, but may have flexible hours based on meetings and clinical trial requirements. The position will interface with patients and collect samples as required for projects. All are welcome Oregon Health & Science University values a diverse and culturally competent workforce. We are proud of our commitment to being an equal opportunity, affirmative action organization that does not discriminate against applicants on the basis of any protected class status, including disability status and protected veteran status. Individuals with diverse backgrounds and those who promote diversity and a culture of inclusion are encouraged to apply. To request reasonable accommodation contact the Affirmative Action and Equal Opportunity Department at ************ or *************.

Assistant Manager The Assistant Manager role at Ambrosia QSR supports the overall operations of a single restaurant. Assistant Managers must have open availability, work full-time, and be scheduled to work shifts that complement the General Manager's schedule (opposing days and shifts). They serve as the right hand to the General Manager and will participate in ongoing development training to foster internal growth within the company. Assistant Managers should possess strong coaching skills, be proficient in all workstations, and have a solid understanding of shift control responsibilities. They must also be capable of handling administrative tasks as requested. Job Responsibilities Team * Recruit, train, and develop new and existing team members while adhering to training plans, procedures, and systems established to meet targeted goals * Coordinate team meetings, including pre-shift and safety committee meetings * Lead by example, fostering a "guest first" mindset and outstanding service * Ensure compliance with all applicable local, state, and federal regulations, including but not limited to break laws, minor employment laws, safety policies, sick leave policies, timekeeping, and scheduling * Ensure a safe and inclusive work environment free from harassment, discrimination, and retaliation, and promptly report any concerns or complaints to the General Manager and Human Resources Guests * Greet every guest warmly and promptly, creating a welcoming atmosphere * Strive to provide an exceptional experience for every guest on every visit, addressing any issues with positivity and sound judgment * Regualarly walk through the resteaurant to check on guests, inquire about their dining experience, and ensure the building's interior and exterior is inviting and safe * Stay informed about the local market trends and community needs to make guest-centric decisions Operations * Oversee compliance with all food safety regulations and restaurant safety procedures, with clear postings as required * Adhere to local marketing plans, ensuring staff are properly trained and prepared for promotions using materials provided by the franchisor * Enforce policies, procedures, and best practices to maintain a safe and positive work environment * Ensure daily food safety standards and operational procedures are consistently met * Maintain open communication with the general manager and leadership as needed Profitability * Ensure all food is prepared fresh to order, following company recipes, and accurately record all items in the POS system * Oversee inventory management by performing regular stock checks and placing orders as needed, while maintaining cost standards * Monitor staffing levels throughout the day to ensure accurate payroll and timekeeping * Manage labor costs to maximize profitability while maintaining employee productivity * Oversee proper use of equipment, small wares, and products * Conduct regular equipment functionality checks and enforce safety rules and regulations * Follow company policies and procedures for cash handling to ensure accuracy, security, and compliance with financial guidelines Education and Work Experience * High school diploma or equivalent * Serv Safe training & certificate * Prior experience with a POS System * 1-2 years of hands-on food or retail management experience Qualifications and Skills * Authorized to work in the United States * Must be at least 18 years of age * Ensure compliance with all required training as mandated by local, state, and federal laws, as well as company policies, to maintain operational and regulatory standards * Maintain a working cell phone and effectively communicate via text, phone calls and emails * Intermediate or higher proficiency in Microsoft 365 * Strong communication and leadership skills, with the ability to collaborate effectively * A responsible team player, demonstrating punctuality, proper attire, and respect for others * Experience in a fast-paced office environment with shifting priorities is a plus * Engage in hands-on leadership with a strong focus on growth and development of people * Be able to work with, coach, and develop a diverse group of people from different backgrounds and with varying strengths * Demonstrate the core Cultural Foundations of Energy, Engagement, Empathy, and Execution through all interactions with both internal and external stakeholders Work Environment and Physical Requirements The work environment is fast-paced, high-energy, and dynamic, requiring the ability to multitask and remain organized under pressure. You will be working in a team-oriented atmosphere, collaborating with other members of the team to ensure smooth restaurant operations. This role involves frequent interaction with customers, creating a welcoming and efficient dining experience. The restaurant environment includes both indoor and outdoor areas, and you may be required to stand, walk, and move throughout the shift. Safety and cleanliness are top priorities, and all staff members are expected to follow health and safety protocols. Flexibility in working hours, including nights, weekends, and some holidays, is required. REQUIRED Personal Protective Equipment (PPE): Boots (oil/heat resistant for fryer filter) Gloves (oil/heat resistant for fryer filter) Apron (oil/heat resistant for fryer filter) Face Shield (oil/heat resistant for fryer filter) Heat Resistant Gloves (oil/heat resistant for fryer filter) Cut Resistant Gloves (slicing equipment) Oven Mitts (heat resistant for ovens) Broiler Gloves (heat resistant for ovens) Benefits * Medical - United Healthcare and Kaiser * Voluntary Life Insurance, Dental and Vision - United Healthcare * Company Paid Life Insurance - United Healthcare Flexible Spending Accounts - Medical, Limited Dental & Vision, Dependent Day Care * Matching 401(K) and Roth retirement savings plans - age 20 or above * Vacation Time - 10 days a year * Floating Holidays - 3 days a year * Sick Time - 1 hour for every 30 hours worked, no waiting period * Direct Deposit * Monthly Bonus Quarterly Bonus * Flexible Scheduling Growth Opportunities * Complimentary meal for each shift worked The information provided here is not intended to be a comprehensive list of the job duties and responsibilities, nor is it intended to cover all the necessary skills for the position. Management reserves the right to assign or reassign duties at any time. The responsibilities outlined in this may change as needed. This Assistant Manager supersedes any earlier versions approved by Ambrosia QSR. It is not intended to create a written or implied employment contract. Ambrosia QSR operates as an at-will employer, meaning either the company or the employee can terminate the employment relationship at any time, with or without cause. Ambrosia QSR is an equal opportunity employer. I acknowledge that I have received and reviewed the Assistant Manager job description and understand that I am responsible for effectively carrying out the essential functions outlined, regardless of any circumstances described. Employee Signature _________________________________________ Employee Name _________________________ Date _______________

The Molecular Vision Laboratory is a medical diagnostic laboratory providing state of the art genetic and genomic diagnostic tests. Our laboratory originated from the Casey Molecular Diagnostic Laboratory at the Oregon Health and Science University where our team of laboratory director, lab technicians and bioinformatics scientists performed genetic and genomic diagnostic tests for over five years. We have recently moved out of the University system and established a diagnostic laboratory open to the broad medical and research community and continue our dedication to the translation of the cutting edge research to clinical care. Job Description Molecular Vision Lab is seeking laboratory research associates/ assistants to join our rapidly growing clinical services laboratory. RESPONSIBILITIES · Carefully execute detailed standard operating procedures in a CLIA certified laboratory including sequence library preparation, hybridization assays, and DNA quality analysis. · Implement quality management procedures, LIMS tracking, data entry, protocol/process deviation documentation. · Carry out DNA molecular methods including DNA isolation, PCR, qPCR, dd PCR and NGS. · Produce, analyze, document and report results, achieving high quality data in a timely manner. · Proactive, troubleshoot, rapidly propose solutions and/or seek help. · Work neatly, keep lab bench and storage areas clean. · Adjust and adapt to new SOPs and workflows as throughput capacity grows. · Professionally handle the pressure of aggressive deadlines while maintaining data quality. · Flexible hours and open to working on weekends if necessary. · Demonstrated organizational abilities and capable of successfully carrying out a variety of detailed tasks. · Support supply and reagent inventory management. Qualifications · BS/MS in molecular biology, biochemistry, genetics or related field. · Demonstrated experience with molecular methods including DNA isolation, fragmentation, PCR, qPCR, dd PCR and NGS library preparation. · Must have excellent organizational skills and be able to maintain careful attention to detail. · Strong verbal and written communication skills. · Demonstrated experience keeping accurate and detailed laboratory records. · Capable of working independently as well as in a team environment with the ability to analyze, interpret data, recognize quality failures and proactively seek help. · Proficiency with standard software (e.g. Microsoft Office) is required. · Ability to thrive in a demanding start-up environment with a positive, productive, professional attitude. · Experience in a high throughput molecular lab or services lab is desirable. · Experience with automated liquid handling platforms is a plus. · Must be a US citizen or have been lawfully admitted for permanent residence. Individuals on temporary or student visas are not eligible. Additional Information All your information will be kept confidential according to EEO guidelines.

The Senior Research Assistant I (SRA I) will assist in the technical management of two transportation data projects that archive diverse transportation data sources and provide access and analysis through a website to transportation professionals. The SRA I will also help with: * performing basic statistical analyses; * managing and maintaining our databases; and * coordinating and developing data collection procedures. The two transportation data projects are PORTAL and BikePed Portal. PORTAL is the official Portland-Vancouver Metropolitan regional transportation data archive. It provides a centralized database that facilitates the collection, archiving, and sharing of data and information for the region's transportation agencies. Data sources include 20- second granularity loop detector data from freeways throughout the Portland-Vancouver area, arterial signals, travel time, freight volumes, transit, incidence, VAS/VMS message, and weather data. Many of these data sources are received by PORTAL in real-time. BikePed Portal is a national non-motorized count data archive. Like PORTAL it is a centralized database that collects, archives, and shares data for public agencies, researchers, educators, and other curious members of the public. Managing these two projects, and future transportation data projects, require that the SRA I assist with the management and performance of all back-end development. Some front-end experience is desirable but not immediately necessary. PORTAL and BikePed Portal use PostgreSQL to store data. The 28+ terabyte database consists of hundreds of tables varying in sizes from a few gigabytes to a few terabytes. The data comes from approximately 10 transportation agencies and is transferred via API and secure data transfer methods. The SRA I will assist with managing or maintaining the data feeds and the data in the database, and help build and design any additional data architecture needed to continue current and future data projects. In addition to the database, PORTAL and BikePed Portal provide web sites where users can access and visualize the data so some front-end experience or familiarity is desirable but not necessary. We expect this position to grow with increasing responsibility. Position Duties/Responsibilities: * Database and Website Management (90%) The SRA I will be responsible for helping with managing or maintaining the data feeds and the data in the database. In addition to the database, PORTAL and BikePed Portal provide web sites where users can access and visualize the data. The SRA I will help manage and maintain primarily the back-end the web interface with some front-end work, and help in developing new analysis and visualization applications and tools for both projects. * Other duties assigned (10%) Other duties assigned at the discretion of the supervisor, which may include troubleshooting and some management of other web related projects that may come up.