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Remote Mri Research Jobs in Oregon (NOW HIRING)

Care Access

Central Study Coordinator I

OR · On-site +1

The Central Study Coordinator (CSC) position combines clinical research and project management ... Ability to work effectively in a remote environment. * Proper home office set-up including a ...

Pollinate

Media Planner I

Portland, OR · On-site +1

... MRI-Simmons, Strata, TapClicks, Looker Studio, etc.) Organizational Responsibilities: * Effective interpersonal skills, interest in research, curious and adaptable as environments change (growth ...

Adswerve, Inc

Digital Media Strategist

OR · On-site +1

$90K - $110K/yr

Work with measurement and research teams to deliver industry insights and relevant performance ... Monthly Remote Work Stipend * New Hire Office Equipment Reimbursement Adswerve is an Equal ...

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Remote Mri Research information

What is a remote MRI researcher?

A Remote MRI Researcher is a professional who conducts research involving Magnetic Resonance Imaging (MRI) from a remote location, rather than working onsite at a hospital or research facility. They analyze MRI data, design experiments, collaborate with medical teams, and may develop or test new imaging techniques, all using digital communication tools and cloud-based platforms. This role is common in academic, clinical, and private research settings where secure data sharing and remote access to imaging software are possible. Remote MRI Researchers often contribute to advancements in medical imaging, neuroscience, and diagnostics while enjoying flexible work arrangements.

What are some common challenges encountered by professionals in remote MRI research roles and how can they be addressed?

Professionals in remote MRI research often face challenges related to data accessibility, communication with multi-site teams, and ensuring compliance with data privacy regulations. Since imaging data is large and sensitive, efficient and secure data transfer protocols are essential. Collaborating remotely requires frequent and clear communication, often through virtual meetings or collaborative platforms, to synchronize research goals and methodologies. Staying updated on institutional and regulatory requirements for remote access and patient confidentiality is also crucial for success in this role.

What are the key skills and qualifications needed to thrive as a remote MRI researcher, and why are they important?

To thrive as a Remote MRI Researcher, you need a strong background in medical imaging, neuroscience, or biomedical engineering, often supported by an advanced degree and experience in MRI data analysis. Familiarity with MRI scanners, image processing software (such as FSL or SPM), and remote collaboration platforms is typically required. Excellent analytical thinking, problem-solving, and communication skills are crucial for interpreting results and coordinating with multidisciplinary teams. These competencies are vital for ensuring high-quality research outcomes and effective collaboration in a remote scientific environment.

What is the difference between Remote Mri Research vs Remote MRI Technologist?

AspectRemote Mri ResearchRemote MRI Technologist
CredentialsTypically requires a research-focused degree, such as a master's or PhD in medical imaging or related fieldRequires ARRT certification and state licensure as an MRI technologist
Work EnvironmentPrimarily research settings, hospitals, or academic institutions, often involving data analysis and study designClinical settings, hospitals, or imaging centers, performing scans and patient positioning remotely
Employer & IndustryResearch institutions, universities, healthcare companiesHospitals, clinics, imaging centers

Remote Mri Research focuses on conducting imaging studies, data analysis, and research projects, often requiring advanced degrees. In contrast, Remote MRI Technologists perform imaging procedures, patient care, and scan operations remotely, requiring certification and clinical experience. Both roles are vital in healthcare but differ in responsibilities, credentials, and work environments.

What are the most commonly searched types of Mri Research jobs in Oregon?

The most popular types of Mri Research jobs in Oregon are:

What are popular job titles related to Remote Mri Research jobs in Oregon?

For Remote Mri Research jobs in Oregon, the most frequently searched job titles are:

What job categories do people searching Remote Mri Research jobs in Oregon look for?

The top searched job categories for Remote Mri Research jobs in Oregon are:

What cities in Oregon are hiring for Remote Mri Research jobs?

Cities in Oregon with the most Remote Mri Research job openings:

Remote Mri Research jobs near you

Central Study Coordinator I

Care Access

OR • On-site, Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 4 days ago

Job description

How This Role Makes a Difference

Central Clinical Services enables decentralized and hybrid clinical trials by providing staff who virtually support patients and sites. The Central Study Coordinator (CSC) position combines clinical research and project management skillsinto a singular role that delivers a strong customer experience for both patients and sites. Often representing Care Access and/or a Care Access client, the CSC acts as a virtual extension of the research site and supports one to four sites concurrently across one or more studies. The CSC is accountable for study delivery at the patient level, including screening, consenting, and conducting protocol mandated study visits, and is expected to coordinate daily work using patient centric practices and a quality-first approach. The CSC also serves as a project manager for their assigned studies with their assigned PIs, helping their sites to stay on top of study deliverables in line with sponsor and CRO expectations. As such, this role will also manage monitoring visits, data management, and query resolution for their assigned sites, and ensure ongoing inspection readiness. This is a mid-to-senior level individual contributor role with the expectation that the CSC has strong working knowledge of and experience in the clinical research industry. 

How You'll Make An Impact
  • Study/Patient Coordination 
    • Perform the Informed Consent process with study participants virtually using e-consent technology. Review all elements of the ICF with the participant and assess their understanding to ensure the protection of human participants in clinical research. Complete signatures using the e-consent platform and register participants in IWRS.
    • Pre-screen and educate potential study participants on the study.  
    • Analyze, understand, and be knowledgeable of the study protocol and the associated disease(s) in combination to be able to educate patients and their families on what participating in the study means for the patient 
    • Interpret patient reported medical history and medication use to determine pre-screening qualification for a study 
    • Manage participant referral portals and study specific applications in real time in accordance with GCP. 
    • Schedule, prepare for, and facilitate participant visits in accordance with the study protocol. This may include overseeing the required scheduling, logistics, technology requirements, and communication applications for participants, central raters, investigators, and other study-related entities such as MRI centers and infusion centers. 
    • Perform protocol mandated visit activities while maintaining GCP compliance 
  • Documentation Management 
    • Maintain all study documentation in accordance with ALCOA-C and across multiple study portals. 
    • Collect sensitive data that is used to determine overall study effectiveness 
    • Create and manage sensitive source documentation for multiple studies including maintaining document security, quality assurance, and secure transmission to clients in a remote environment 
    • Enter data and resolve queries in EDC and other portals within appropriate time window defined by the study 
    • Correctly identify, document, and report Adverse Events and Serious Adverse Events (AEs and SAEs) 
    • Ensure all study trackers and systems are up to date daily 
    • Support site compliance with subject safety reporting 
  • Study Project Management 
    • Manage study work for each assigned site as delegated by the PI, collaborating with multiple sites and site teams concurrently to deliver the highest quality work with each participant for each site. 
    • Requires juggling multiple unique protocols of varying complexity 
    • Host regular calls, acting as the subject matter expert and representative of Care Access, with each assigned PI and present on key elements of the study within CSC scope, which may include a review of new referrals, participants in screening, participants in treatment, data and query progress and issues, upcoming monitoring visits, etc. 
    • Prepare meeting agendas and circulate meeting minutes, follow-up on action items for self and teammates. 
    • Facilitate communication between study site, CRA, and sponsor. 
  • Other Responsibilities
    • Build strong rapport with sites, participants, CRAs, and sponsor contacts. 
    • Make decisions that optimize the experience within the study for the participant, PI, and other site staff. 
    • Perform quality checks for self and others to ensure overall data integrity. 
    • Complete ongoing trainings and adhere to system access guidelines.
    • Analyze and understand study protocols.  
The Expertise Required
Knowledge, Skills, and Abilities
  • Able to navigate and troubleshoot a wide variety of technologies used for clinical research including recruitment platforms, IWRS, EDC, and other clinical trial software, and able to work across multiple platforms at the same time. 
  • Proficient with Microsoft Office applications (Word, Outlook, Teams, and Excel). 
  • Demonstrate professionalism in all situations and work effectively with a diverse group of individuals. 
  • Understand when issues require escalation. 
  • Strong communication customer service abilities 
  • Proficient in research terminology and basic medical terminology 
  • Understand the overall clinical development paradigm and excellent working knowledge of government regulations, GCP, and ALCOA-C 
  • Strong organization and time management skills 
  • High attention to detail 
  • Ability to work in a fast-paced environment. 
  • Critical thinker and problem solver. 
  • Ability to work effectively in a remote environment. 
  • Proper home office set-up including a private space for participant communication and high-speed internet (at minimum: 100MB up and 15 MB down, 5 GHz router)
Certifications/Licenses, Education, and Experience
  • Minimum Education:
    • Bachelor's Degree preferred, or equivalent combination of education, training and experience
  • Minimum Experience:
    • At least 3 years of relevant clinical research experience 
  • Fluency in Spanish is a bonus
  • CCRC preferred
How We Work Together
  • Location: Remote within the United States. This role requires 100% of work to be performed in a remote office environment.
  • Travel: This is a remote position with less than 10% travel requirements. Occasional planned travel may be required as part of the role.
  • Physical demands associated with this position Include: The ability to use keyboards and other computer equipment.

The expected pay range for this role is $75,000 - $95,000 USD per year for full time team members.

Benefits & Perks (US Full Time Employees)
  • Paid Time Off (PTO) and Company Paid Holidays
  • 100% Employer paid medical, dental, and vision insurance plan options
  • Health Savings Account and Flexible Spending Accounts
  • Bi-weekly HSA employer contribution
  • Company paid Short-Term Disability and Long-Term Disability
  • 401(k) Retirement Plan, with Company Match 

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