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Clinical Research Informatics Jobs in Utah (NOW HIRING)

Clinical Informatics - 814 Primary Purpose: The Clinical Informaticist plays a crucial role in ... operations, research, data utilization, and data-driven decision making. About ARUP: ARUP ...

2025 Fall Intern, Clinical Applications

Orem, UT · On-site

$13 - $17.50/hr

... in clinical research, primarily the Clinical Trial Management System (CTMS). How You'll Create ... Pursuing a bachelor's degree in Computer Science, Information Systems, Health Informatics, Data ...

2025 Fall Intern, Clinical Applications

Ogden, UT · On-site

$14.75 - $19.50/hr

... in clinical research, primarily the Clinical Trial Management System (CTMS). How You'll Create ... Pursuing a bachelor's degree in Computer Science, Information Systems, Health Informatics, Data ...

$13 - $17.25/hr

... in clinical research, primarily the Clinical Trial Management System (CTMS). How You'll Create ... Pursuing a bachelor's degree in Computer Science, Information Systems, Health Informatics, Data ...

$13 - $17.50/hr

... in clinical research, primarily the Clinical Trial Management System (CTMS). How You'll Create ... Pursuing a bachelor's degree in Computer Science, Information Systems, Health Informatics, Data ...

$14 - $18.75/hr

... in clinical research, primarily the Clinical Trial Management System (CTMS). How You'll Create ... Pursuing a bachelor's degree in Computer Science, Information Systems, Health Informatics, Data ...

$14.75 - $19.50/hr

... in clinical research, primarily the Clinical Trial Management System (CTMS). How You'll Create ... Pursuing a bachelor's degree in Computer Science, Information Systems, Health Informatics, Data ...

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Showing results 1-20

Clinical Research Informatics information

See Utah salary details

$47.3K

$94.3K

$149.3K

How much do clinical research informatics jobs pay per year?

As of Aug 5, 2026, the average yearly pay for clinical research informatics in Utah is $94,311.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,300.00 and $105,100.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in clinical research informatics?

Excelling in Clinical Research Informatics requires a solid background in clinical research methodologies, health informatics, data management, and often a relevant degree such as in biomedical informatics or computer science. Proficiency with data analysis tools (like SAS, R, or Python), electronic data capture systems (such as REDCap), and knowledge of healthcare regulatory standards (HIPAA, GCP) are typically expected. Strong communication, analytical thinking, and the ability to collaborate across multidisciplinary teams are important soft skills. These competencies ensure effective collection, management, and interpretation of clinical data, supporting high-quality research outcomes and regulatory compliance.

What is clinical research informatics?

A Clinical Research Informatics job involves managing and analyzing healthcare data to support clinical research and improve patient outcomes. Professionals in this field develop and maintain databases, ensure data integrity, and utilize informatics tools to streamline clinical trials. They collaborate with researchers, clinicians, and IT specialists to optimize data collection, integration, and analysis. This role requires knowledge of biomedical research, data science, and regulatory compliance.

What does a clinical research informatics specialist do?

Professionals in Clinical Research Informatics are usually responsible for designing and managing databases for clinical studies, ensuring data integrity, and analyzing research data to support scientific findings. They often coordinate with clinical researchers, IT specialists, and regulatory teams to develop data collection protocols and maintain compliance with industry standards. Regular tasks may include troubleshooting data issues, preparing reports, and training staff on informatics systems. This role often involves both independent work and close collaboration with multidisciplinary teams, offering a dynamic and impactful work environment.

What are popular job titles related to Clinical Research Informatics jobs in Utah? For Clinical Research Informatics jobs in Utah, the most frequently searched job titles are:
What cities in Utah are hiring for Clinical Research Informatics jobs? Cities in Utah with the most Clinical Research Informatics job openings:
Infographic showing various Clinical Research Informatics job openings in Utah as of July 2026, with employment types broken down into 2% As Needed, 78% Full Time, 14% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $94,311 per year, or $45.3 per hour.

Feasibility Informatics Manager

Icon plc

Salt Lake City, UT

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 5 days ago


Job description

Feasibility Informatics Manager

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


Title: Feasibility Informatics Manager

Role Summary:

To serve as a technical feasibility strategy expert, leading and managing the process of clinical project feasibility in support of proposal teams by assisting Business Development with the generation of cost proposals, providing input and advice relating to operational strategy, and supporting client interactions and long-term strategic partnerships.

To perform as a technical expert in the feasibility strategy development process for internal (e.g., to Business Development Operations) and external clients (e.g., Sponsors), providing strategic input. This includes, but is not limited to:

  • Serving as an expert resource to project teams for feasibility strategy and informatics services (e.g., feasibility during rescue situations).

  • Providing support during bid defense (or potential preferred partner) meeting preparation and attending/presenting at bid defense (or potential preferred partner) meetings.

  • Providing handover to awarded site identification (site ID) team of all relevant feasibility strategy proposed during RFP process, followed by End of Site ID analysis to be performed.

To lead the process of clinical project feasibility during standalone feasibility (awarded) projects by managing and being accountable for the delivery of all awarded projects assigned to the individual. This includes, but is not limited to, accountability for all recommendations for next steps with assessment of risks and strategies to manage risks to the project delivery.

Responsibilities:

  • Recognize, exemplify, and adhere to ICON's values (Collaboration, Integrity, Inclusion, and Agility) which center around our commitment to people, clients, and performance.

  • Recognize the importance of and create a culture of process improvement with a focus on streamlining our processes, adding value to our business and meeting client needs. This includes participation in active sharing of FIM learning across therapeutic teams with a purpose to improve strategic feasibility support and outputs (e.g., leveraging resources and tools, slide development, user-acceptance testing for tools).

  • Travel (approximately 20%) domestic and/or international as needed.

  • The FM will maintain communication and relationships between all relevant parties to ensure that available intelligence is utilized to deliver optimal, data-driven feasibility strategy solutions. Relevant parties include, but are not limited to: Proposal team members, Project Managers/Strategy Leads, Patient Recruitment & Retention Specialists, Site Identification Managers/Leads, Therapeutic Experts, Therapeutically Aligned clinical teams (as assigned), Business Development Associates, Sponsors, Quality Assurance Associates, and other internal/external experts.

In performing the above essential functions, the remit includes, but is not limited to:

Preparation of feasibility data by:

  • Collecting data from data assets as well as country associates, site level Investigators, and KOL interviews when required.

  • Determining site profile.

  • Developing appropriate feasibility strategies, including approach and management for standalone feasibilities.

  • Providing full documentation in the proposal that may include incidence/prevalence, treatment practices, reimbursement practices, competitive landscape, enrollment trend analysis, etc.

  • Collaborating with Patient Recruitment, Start-up, and other teams as needed.

  • Ensuring feasibility data is fully evaluated to determine risks to project delivery and that any risks identified are appropriately escalated and solutions planned/discussed within the feasibility strategy (e.g., alternative scenario).

  • Transitioning all pre-award generated data (including strategy) to the Site ID Manager/Lead (with involvement of awarded project team) upon award.

  • Preparing internal project information to support ad hoc requests for information (e.g., early engagement, pre-award, post-award).

Conduct of evidence-based feasibility by:

  • Establishing viability of proposed project through interrogation of internal and external performance metrics (e.g., previous feasibility data, Industry intelligence, EMR/EHR and RWE data) and resources to establish demographics and data on patient populations.

  • Ensuring all collected data is high-quality, accurate, and fully documented in the ICON feasibility business systems.

  • Performing accurate and correct data analysis and interpretation to support feasibility strategy solutions.

Preparation for and attendance at bid defense meetings (by phone or in person) by:

  • Supporting and/or presenting strategic project planning.

Performing as a functional lead with accountability for delivery of high-quality feasibility standalone services (awarded/contracted) by:

  • Initiating, conducting, coordinating, analyzing, and reporting feasibility studies as contracted on time and on budget (managing staff resources).

  • Meeting Sponsor objectives and expectations.

  • Coordinating with the Site ID Lead per RACI.

  • Developing appropriate country and site selection strategies and analyzing/interpreting results to provide protocol feedback and to make appropriate country and site recommendations based on objective analysis (e.g., ranking).

  • Documenting and tracking feasibility study results.

What you need:

  • Master's Degree

  • 6-9 years of experience in a Clinical Research environment


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.

Are you a current ICON Employee? Please click here to apply