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Biotech Communications Jobs in Utah (NOW HIRING)

CRA 1, IQVIA Biotech

Pleasant View, UT · On-site

$71K - $145K/yr

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have ... A central part of this role involves building and maintaining strong communication with ...

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have ... A central part of this role involves building and maintaining strong communication with ...

CRA 1, IQVIA Biotech

Pleasant View, UT · On-site

$71K - $145K/yr

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have ... A central part of this role involves building and maintaining strong communication with ...

CRA 1, IQVIA Biotech

Salt Lake City, UT · On-site

$71K - $145K/yr

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have ... A central part of this role involves building and maintaining strong communication with ...

BioPharma Account Rep

Salt Lake City, UT · On-site

$85K - $116K/yr

Must be able to communicate pharmacodynamics with physicians as well as other clinical evidence * Strong alignment to our corporate values of patient at center, collaboration, relentless pursuit of ...

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Showing results 1-20

Biotech Communications information

See Utah salary details

$28.2K

$61K

$101.5K

How much do biotech communications jobs pay per year?

As of Aug 22, 2026, the average yearly pay for biotech communications in Utah is $61,000.00, according to ZipRecruiter salary data. Most workers in this role earn between $48,700.00 and $64,600.00 per year, depending on experience, location, and employer.

What is biotech communications?

Biotech communications involves sharing scientific information, research findings, and developments from biotechnology companies or organizations with various audiences, including the public, investors, media, and regulatory bodies. Professionals in this field translate complex scientific concepts into clear, accessible messages to build understanding and trust. Their work may include writing press releases, managing social media, developing educational materials, and coordinating with scientists and stakeholders to ensure accurate representation of biotechnological advances.

How does a biotech communications professional typically collaborate with scientists and researchers to ensure accurate messaging?

Biotech Communications professionals work closely with scientists and researchers to translate complex scientific data into clear, accessible messaging for various audiences. This often involves attending research meetings, reviewing scientific materials, and conducting interviews with subject matter experts to ensure accuracy. Regular collaboration helps bridge the gap between technical research and public understanding, making it essential for communicators to be both scientifically literate and skilled in storytelling. Teamwork is key, as effective communication can directly impact a company’s reputation, regulatory compliance, and stakeholder engagement.

What are the key skills and qualifications needed to thrive in biotech communications, and why are they important?

To excel in Biotech Communications, you need a background in life sciences or biotechnology combined with strong writing, editing, and public relations skills, often supported by a degree in communications or a related field. Familiarity with scientific publishing platforms, media monitoring tools, and data visualization software is typically required. Exceptional interpersonal, storytelling, and adaptability skills help professionals explain complex scientific concepts to diverse audiences and manage stakeholder relationships. These competencies are vital for ensuring accurate, accessible communication of scientific advances and fostering trust among the public, media, and industry partners.

What is the difference between Biotech Communications vs Scientific Writer?

AspectBiotech CommunicationsScientific Writer
Required CredentialsBachelor's or master's in life sciences, communications, or related fieldsBachelor's or master's in life sciences, journalism, or related fields
Work EnvironmentPharmaceutical or biotech companies, agencies, or freelanceResearch institutions, publishing, or biotech companies
Employer & Industry UsageUsed for creating marketing, educational, and regulatory contentFocused on producing research articles, reports, and manuscripts

Biotech Communications professionals primarily develop marketing, educational, and regulatory content within biotech and pharmaceutical industries, often requiring communication skills alongside scientific knowledge. Scientific Writers focus on creating detailed research documents and publications, emphasizing scientific accuracy. While both roles require a background in science, Biotech Communications emphasizes communication skills and industry knowledge, whereas Scientific Writers concentrate on technical writing and research dissemination.

Infographic showing various Biotech Communications job openings in Utah as of August 2026, with employment types broken down into 100% Full Time. Highlights an 46% In-person, 27% Hybrid, and 27% Remote job distribution, with an average salary of $61,000 per year, or $29.3 per hour.

CRA 1, IQVIA Biotech

IQVIA

Pleasant View, UT • On-site

$71K - $145K/yr

Full-time

Re-posted 8 days ago


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

63rd of 225 rated it services


Job description

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 highquality 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 closeout 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 sitelevel 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 startup activities based on study needs.

Accurate and timely documentation is critical. The CRA I prepare detailed monitoring visit reports, followup 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 athttps://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 - $145,300.00. 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.

What IQVIA employees say

Pay

Benefits

Hours and flexibility

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US