ZipRecruiter

Log In

2

Full Time Non Clinical Radiologist Jobs (NOW HIRING)

MMS

Nonclinical Writer

Canton, MI · On-site

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 ...

Radiology Partners

General Radiologist

Toledo, OH

$447K - $1M/yr

Opportunities to grow in both clinical and non-clinical roles within the practice Compensation ... Day/1st Shift * Full-time (30+ hrs/week) Requirements * Licensed or have the ability to be licensed ...

MMS Holdings Inc.

Nonclinical Writer

Canton, MI · On-site

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

Boston, MA · On-site

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

Raleigh, NC · On-site

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 ...

Radiology Partners

General Radiologist

Tucson, AZ · On-site

$500K - $550K/yr

This full-time, onsite position offers a partnership track opportunity and involves a diverse case ... The role provides an opportunity to grow in both clinical and non-clinical capacities within the ...

Radiology Partners

Remote Daytime Neuro Radiologist

$327K - $409K/yr

... seeking full-time and part-time remote radiologists to support our growing practice onsite ... Opportunities to grow in both clinical and non-clinical roles within the practice DESIRED ...

Sodexo

Caregiver - Non Clinical

Fremont, CA · On-site

$24 - $29/hr

Caregiver - Non Clinical Location: SISTERS OF THE HOLY FAMILY, FREMONT - 13535002 Workdays/shifts ... Employment Type: Full-time Pay Range: $24 - $29 Working with Sodexo is more than a job; it's a ...

Sodexo

Caregiver - Non Clinical

Fremont, CA · On-site

$24 - $29/hr

Caregiver - Non Clinical Location: SISTERS OF THE HOLY FAMILY, FREMONT - 13535002 Workdays/shifts ... Employment Type: Full-time Pay Range: $24 per hour - $29 per hour Working with Sodexo is more than ...

next page

Showing results 1-20

All Jobsfull time JobsFull Time Non Clinical Radiologist Jobs

Full Time Non Clinical Radiologist information

See salary details

$50K

$345K

$400K

How much do full time non clinical radiologist jobs pay per year?

As of Aug 21, 2026, the average yearly pay for full time 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 is the difference between Full Time Non Clinical Radiologist vs Diagnostic Radiologist?

AspectFull Time Non Clinical RadiologistDiagnostic Radiologist
CredentialsMedical degree, radiology residency, board certificationMedical degree, radiology residency, board certification
Work EnvironmentResearch, teaching, administrative roles, imaging interpretationImaging interpretation, diagnosis, patient consultations
Employer & Industry UsageHospitals, academic institutions, research centersHospitals, clinics, imaging centers

Full Time Non Clinical Radiologists focus on research, teaching, and administrative tasks, often working in academic or research settings. Diagnostic Radiologists primarily interpret medical images to diagnose patient conditions in clinical environments. Both roles require similar credentials but differ in daily responsibilities and work settings.

More about Full Time Non Clinical Radiologist jobs

What cities are hiring for Full Time Non Clinical Radiologist jobs?

Cities with the most Full Time 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 job categories do people searching Full Time Non Clinical Radiologist jobs look for?

The top searched job categories for Full Time Non Clinical Radiologist jobs are:

Full Time Non Clinical Radiologist jobs near you
Infographic showing various Full Time Non Clinical Radiologist job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $344,970 per year, or $165.9 per hour.

Nonclinical Writer

MMS

Canton, MI • On-site

Full-time

Re-posted 23 days ago

Job description

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). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
 
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.
This person will participate in the development, writing, and management of highly technical nonclinical documents. 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, Investigator’s Brochure [IB], Nonclinical Study Reports, Meeting Requests, Briefing Documents, RTQs)
  • Lead projects independently with minimal oversight, lead the writing (structure, content and messaging) of nonclinical documents, ensure the nonclinical package aligns with current regulatory guidelines and meets scientific integrity
  • Ability to author based on highly technical sources such as GLP and non-GLP nonclinical study reports, in vivo and in vitro nonclinical data
  • Ability to develop a mapping plan for the placement of nonclinical studies within structure of Module 2.4 and 2.6 eCTD submission documents
  • Interpret and analyze applicable pharmacokinetics, pharmacology, and toxicology data (eg, 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
  • Ability to complete documents according to sponsor’s format, processes, and according to regulatory guidelines
  • Ability to effectively operate in an environment that requires negotiation, persuasion, collaboration, and analytical judgment
  • Organizational expert within the nonclinical subject area
  • Excellent written/oral communication and strong time and project management skills
  • Ability to attend regular team meetings, lead client meeting and CRMs
  • Ability to work in various client systems (eg, SharePoint, Veeva RIM, PleaseReview, EndNote), templates and toolbars
  • Strong understanding of regulatory guidances as it applies to nonclinical submission documents and drug development (eg, 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

Powered by JazzHR

JWVqDeM8oN

M. M. S. logo

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

View All M. M. S. Jobs