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Remote Non Clinical Radiologist Jobs (NOW HIRING)

MMS

Nonclinical Writer

Toledo, OH · Remote

This is a full‐time, remote position. Roles and Responsibilities Strong experience with development and writing of nonclinical documents (e.g., Module 2.4 and 2.6 eCTD submission documents ...

MMS

Nonclinical Writer

Richmond, VA · Remote

This is a full‐time, remote position. Roles and Responsibilities Strong experience with development and writing of nonclinical documents (eg, Module 2.4 and 2.6 eCTD submission documents ...

W3Global Inc.

Remote Radiologist

New York, NY · Remote

$350K - $450K/yr

Radiology / Clinical Services (Position Summary) The company is seeking a highly qualified Remote Radiologist to provide timely, accurate, and high-quality diagnostic imaging interpretations for our ...

MMS

Nonclinical Writer

Seattle, WA · On-site +1

$70K - $85K/yr

This is a full-time, remote position.Roles and ResponsibilitiesStrong experience with development and writing of nonclinical documents (eg, Module 2.4 and 2.6 eCTD submission documents, Investigator ...

MMS

Nonclinical Writer

Bridgeport, CT · Remote

This is a full‐time, remote position. Roles and Responsibilities Strong experience with development and writing of nonclinical documents (eg, Module 2.4 and 2.6 eCTD submission documents ...

New

MMS

Nonclinical Writer

Richmond, VA · Remote

This is a full‐time, remote position. Roles and Responsibilities Strong experience with development and writing of nonclinical documents (eg, Module 2.4 and 2.6 eCTD submission documents ...

MMS

Nonclinical Writer

Denver, CO · Remote

This is a full‐time, remote position. Roles and Responsibilities Strong experience with development and writing of nonclinical documents (e.g., Module 2.4 and 2.6 eCTD submission documents ...

Radiology Partners

Remote Late Night Neuro Radiologist

$327.60K - $409.40K/yr

... Radiology Corporation (CRC) is seeking full-time remote neuroradiologists to support our growing ... Opportunities to grow in both clinical and non-clinical roles within the practice DESIRED ...

MMS

Nonclinical Regulatory Writer (Remote)

Seattle, WA · Remote

$70K - $85K/yr

A clinical research organization is seeking an entry-level regulatory writer to join their innovative team in Seattle. This full-time, remote position involves developing and managing nonclinical ...

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How much do remote non clinical radiologist jobs pay per year?

As of Jun 3, 2026, the average yearly pay for remote non clinical radiologist in the United States is $344,970.00, according to ZipRecruiter salary data. Most workers in this role earn between $320,000.00 and $400,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Remote Non Clinical Radiologist, and why are they important?

To excel as a Remote Non Clinical Radiologist, you need a medical degree with specialty training in radiology, a valid medical license, and expertise in interpreting medical images. Familiarity with Picture Archiving and Communication Systems (PACS), teleradiology software, and standardized reporting systems is essential. Strong attention to detail, critical thinking, and effective written communication are vital soft skills for providing accurate consults and reports remotely. These competencies ensure precise diagnoses, efficient workflow, and high-quality patient care in a virtual setting.

How does a remote non-clinical radiologist typically collaborate with clinical teams and other healthcare professionals?

Remote non-clinical radiologists often work closely with clinical teams through secure digital platforms, providing expert consultation, second opinions, and supporting quality assurance initiatives. Communication is typically facilitated via video conferences, emails, or specialized medical software, allowing for timely feedback and information sharing. Building strong relationships with referring physicians, technologists, and administrative staff is essential, as it ensures efficient workflow and accurate interpretation of imaging data. While there is less face-to-face interaction, strong communication skills and responsiveness are key to effective collaboration in this remote environment.

What is a Remote Non Clinical Radiologist?

A Remote Non Clinical Radiologist is a medical professional with radiology training who works outside of traditional clinical settings, often from home or another remote location. Instead of diagnosing patients directly, they may focus on tasks such as consulting, research, teaching, medical imaging analysis for research or AI development, or providing expertise for insurance or legal cases. This role allows radiologists to use their expertise without direct patient care, offering greater flexibility and often better work-life balance. The demand for remote non clinical radiologists has increased with advancements in technology and telemedicine.
More about Remote Non Clinical Radiologist jobs
What cities are hiring for Remote Non Clinical Radiologist jobs? Cities with the most Remote Non Clinical Radiologist job openings:
What are the most commonly searched types of Non Clinical Radiologist jobs? The most popular types of Non Clinical Radiologist jobs are:
What states have the most Remote Non Clinical Radiologist jobs? States with the most job openings for Remote Non Clinical Radiologist jobs include:
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Remote Non Clinical Radiologist jobs near you
Infographic showing various Remote Non Clinical Radiologist job openings in the United States as of May 2026, with employment types broken down into 12% As Needed, 6% Full Time, 52% Part Time, and 30% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $344,970 per year, or $165.9 per hour.

Nonclinical Writer

MMS

Toledo, OH • Remote

Full-time

Posted 19 days ago

Job description

Join to apply for the Nonclinical Writer role at MMS . Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO).

With a global footprint across four continents, MMS maintains an industry‐leading customer satisfaction rating and fosters a collaborative and inclusive work environment where employees can thrive. This is a full‐time, remote position. Roles and Responsibilities Strong experience with development and writing of nonclinical documents (e.g., Module 2.4 and 2.6 eCTD submission documents, Investigator's Brochure [IB], Nonclinical Study Reports, Meeting Requests, Briefing Documents, RTQs) Lead projects independently with minimal oversight, leading the writing (structure, content and messaging) of nonclinical documents, ensuring the nonclinical package aligns with current regulatory guidelines and meets scientific integrity Author based on highly technical sources such as GLP and non‐GLP nonclinical study reports, in vivo and in vitro nonclinical data Develop a mapping plan for the placement of nonclinical studies within the structure of Module 2.4 and 2.6 eCTD submission documents Interpret and analyze applicable pharmacokinetics, pharmacology, and toxicology data (e.g., Prism files, bioanalytical reports, clinical pathology reports, PK/TK evaluation reports) Collaborate with cross‐functional teams such as project management, safety, efficacy, biostats, regulatory operations, and CMC Demonstrated ability to lead others to complete complex projects Complete documents according to sponsor's format, processes, and regulatory guidelines Operate effectively in an environment requiring negotiation, persuasion, collaboration, and analytical judgment Serve as an organizational expert within the nonclinical subject area Exhibit excellent written and oral communication and strong time and project management skills Attend regular team meetings, lead client meetings and CRMs Work in various client systems (e.g., SharePoint, Veeva RIM, PleaseReview, EndNote), templates and toolbars Have a strong understanding of regulatory guidances as it applies to nonclinical submission documents and drug development (e.g., ICH, FDA and EMA regulations and guidelines, GLP, GCP, GMP and GDP) Requirements BS+ in pharmacology, toxicology, biology or chemistry, or related field, with industry experience within regulatory writing, regulatory affairs, laboratory sciences, quality assurance/control Knowledge of GLP, ICH guidelines, and applicable regulatory requirements 2+ years of pharmaceutical regulatory nonclinical writing experience Strong writing and analytical skills Proficiency with MS Office applications Hands‐on experience with clinical trial and pharmaceutical development preferred Basic understanding of CROs and scientific & nonclinical data/terminology, & the drug development process #J-18808-Ljbffr

About M. M. S.

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1 - 10 Employees

Headquarters location

Los Angeles, CA, US

Year founded

1980

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