Top 17 research scientist Jobs in ogden ut

CRA 1, IQVIA Biotech
IQVIA —Pleasant View, UT
- $71,900 - $119,900 a year
- Full-time
- Bachelor's degree
- Travel
- Communication skills
Medical Lab Scientist
Tanner Clinic —Layton, UT
- Part-time
- Mid-level
- Ability to lift 50 pounds
- Cleaning
Quick Apply
R&D Scientist
Alphia —Ogden, UT
- 5 years
- Bachelor of Science
- Bachelor's degree
Quick Apply
Research/Principal Research Scientist Level 2/3
Northrop Grumman —Clearfield, UT
- $79,300 - $184,200 a year
- Overtime
- Office
- Master's degree
- Doctor of Philosophy
- Paid holidays
- Disability insurance
Product Development and Research Manager
Growve —Ogden, UT
- Full-time
- 5 years
- Mid-level
- Master's degree
- Health insurance
- 401(k)
Quick Apply
10d
Principal/Sr. Research Scientist Level 3/4
Northrop Grumman —Clearfield, UT
- $98,400 - $184,200 a year
- Overtime
- Office
- Master's degree
- Doctor of Philosophy
- Paid holidays
- Disability insurance
MA English Graduate Research Assistant
Weber State University —Ogden, UT
- $15 an hour
- Part-time
- Background check
- Office
- University
Advanced Composites Lab Operations Manager
University of Dayton —Layton, UT
- Full-time
- 6 years
- University
- Bachelor's degree
- Health insurance
- Dental insurance
Director, Gene Therapy Clinical Science
Rocket Pharmaceuticals —United States
- $206,000 - $270,000 a year
- Full-time
- Nursing
- 11+ years
- Bachelor of Science in Nursing
- Paid holidays
- Health insurance
Applied Scientist - AI Trainer
DataAnnotation —United States
- $40 - $60 an hour
- Part-time
- Remote
- Computer Science
- Writing skills
- English
- Flexible schedule
Quick Apply

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AI Data Quality Specialist - AI Trainer
DataAnnotation —Salt Lake City, UT
A bachelor's degree in a quantitative field is preferred (Statistics, Computer Science, Mathematics, Engineering, or similar); a master's or PhD is a plus.
$40 - $60 an hour
Quick Apply
Private Banker - AI Trainer
DataAnnotation —South Jordan, UT
Proficient in financial analysis, financial modeling, portfolio theory, valuation, and data analysis. You will measure the progress of these AI chatbots,…
$50 - $60 an hour
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Lab Technician
Buckeye Clinic —Dublin, OH
This position offers an exciting opportunity to contribute to innovative scientific research within a regulated environment while developing your expertise in…
$23.52 - $28.32 an hour
Quick Apply
Post-Doctoral Scholar- Medical Oncology
The Ohio State University Wexner Medical Center —Columbus, OH
Develop independent, hypothesis-driven research programs Publish in high-impact journals Lead and contribute to competitive grant and fellowship applications (…

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CRA 1, IQVIA Biotech

IQVIA -
Pleasant View, UT

Apply Now

Job Details

Full-time
$71,900 - $119,900 a year

Qualifications

Clinical audit and monitoring
ICH guidelines
Bachelor's degree
Clinical quality assurance standards
Oncology
Stakeholder relationship building

Full Job Description

Pleasant View, United States of America | Full time | Field-based | R1534476

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have experience monitoring in oncology solid tumor.

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.

Job Overview

The Clinical Research Associate I (CRA I) plays a key role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities. In this position, you will ensure that assigned study sites conduct trials in compliance with the protocol, applicable regulations, Good Clinical Practice (GCP), and ICH guidelines. This role is essential in protecting patient safety, ensuring high‑quality clinical data, and maintaining study integrity.

Key Responsibilities

As a CRA I, you will conduct various types of monitoring visits—including site selection, initiation, routine monitoring, and close‑out visits—to evaluate the quality and integrity of site practices. You will verify that study activities are performed according to regulatory requirements and sponsor expectations, escalating quality concerns as necessary. During these visits, you will review essential documents, assess protocol adherence, oversee data entry and query resolution, and ensure maintenance of both the Trial Master File (TMF) and the Investigator Site File (ISF).

A central part of this role involves building and maintaining strong communication with investigative sites. You will provide protocol training, set expectations, address site‑level challenges, and support recruitment planning to help sites meet enrollment targets. You will also collaborate closely with internal project teams to ensure cohesive study execution and may contribute to site-level financial processes or start‑up activities based on study needs.

Accurate and timely documentation is critical. The CRA I prepare detailed monitoring visit reports, follow‑up letters, and all required study documentation to ensure audit readiness and transparent oversight. The ability to manage multiple tasks, prioritize effectively, and work independently while maintaining productive team relationships is essential for success.

Qualifications

Bachelor’s degree required; a scientific or healthcare discipline is preferred.
6 months –2 years of relevant experience, with equivalent combinations of education, training, or completion of a CRA training program considered.
Basic knowledge of clinical research regulations (GCP/ICH).
Ability to travel as required by the project.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $71,900.00 - $119,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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research scientist jobs in ogden ut

CRA 1, IQVIA Biotech

Medical Lab Scientist

R&D Scientist

Research/Principal Research Scientist Level 2/3

Product Development and Research Manager

Principal/Sr. Research Scientist Level 3/4

MA English Graduate Research Assistant

Advanced Composites Lab Operations Manager

Director, Gene Therapy Clinical Science

Applied Scientist - AI Trainer

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