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Biotech Patient Education Jobs (NOW HIRING)

CRA 1, IQVIA Biotech

Bloomington, IL · On-site

$71K - $145K/yr

This role is essential in protecting patient safety, ensuring highquality clinical data, and ... education, training, or completion of a CRA training program considered. * Basic knowledge of ...

CRA 1, IQVIA Biotech

Ithaca, NY · On-site

$71K - $145K/yr

This role is essential in protecting patient safety, ensuring highquality clinical data, and ... education, training, or completion of a CRA training program considered. * Basic knowledge of ...

This role is essential in protecting patient safety, ensuring highquality clinical data, and ... education, training, or completion of a CRA training program considered. * Basic knowledge of ...

CRA 1, IQVIA Biotech

Durham, NC · On-site

$71K - $145K/yr

This role is essential in protecting patient safety, ensuring high-quality clinical data, and ... education, training, or completion of a CRA training program considered. * Basic knowledge of ...

CRA 1, IQVIA Biotech

Indianapolis, IN · On-site

$71K - $145K/yr

This role is essential in protecting patient safety, ensuring highquality clinical data, and ... education, training, or completion of a CRA training program considered. * Basic knowledge of ...

CRA 1, IQVIA Biotech

Rosemont, IL · On-site

$71K - $145K/yr

This role is essential in protecting patient safety, ensuring highquality clinical data, and ... education, training, or completion of a CRA training program considered. * Basic knowledge of ...

CRA 1, IQVIA Biotech

Fort Worth, TX · On-site

$71K - $145K/yr

This role is essential in protecting patient safety, ensuring highquality clinical data, and ... education, training, or completion of a CRA training program considered. * Basic knowledge of ...

CRA 1, IQVIA Biotech

Durham, NC · On-site

$71K - $145K/yr

This role is essential in protecting patient safety, ensuring highquality clinical data, and ... education, training, or completion of a CRA training program considered. * Basic knowledge of ...

This role is essential in protecting patient safety, ensuring highquality clinical data, and ... education, training, or completion of a CRA training program considered. * Basic knowledge of ...

This role is essential in protecting patient safety, ensuring highquality clinical data, and ... education, training, or completion of a CRA training program considered. * Basic knowledge of ...

CRA 1, IQVIA Biotech

Cleveland, OH · On-site

$71K - $145K/yr

This role is essential in protecting patient safety, ensuring highquality clinical data, and ... education, training, or completion of a CRA training program considered. * Basic knowledge of ...

CRA 1, IQVIA Biotech

Chicago, IL · On-site

$71K - $145K/yr

This role is essential in protecting patient safety, ensuring highquality clinical data, and ... education, training, or completion of a CRA training program considered. * Basic knowledge of ...

CRA 1, IQVIA Biotech

Pleasant View, UT · On-site

$71K - $145K/yr

This role is essential in protecting patient safety, ensuring highquality clinical data, and ... education, training, or completion of a CRA training program considered. * Basic knowledge of ...

CRA 1, IQVIA Biotech

Collegeville, PA · On-site

$71K - $145K/yr

This role is essential in protecting patient safety, ensuring highquality clinical data, and ... education, training, or completion of a CRA training program considered. * Basic knowledge of ...

CRA 1, IQVIA Biotech

Henderson, NV · On-site

$71K - $145K/yr

This role is essential in protecting patient safety, ensuring highquality clinical data, and ... education, training, or completion of a CRA training program considered. * Basic knowledge of ...

CRA 1, IQVIA Biotech

Kansas City, MO · On-site

$71K - $145K/yr

This role is essential in protecting patient safety, ensuring highquality clinical data, and ... education, training, or completion of a CRA training program considered. * Basic knowledge of ...

CRA 1, IQVIA Biotech

Las Vegas, NV · On-site

$71K - $145K/yr

This role is essential in protecting patient safety, ensuring highquality clinical data, and ... education, training, or completion of a CRA training program considered. * Basic knowledge of ...

CRA 1, IQVIA Biotech

San Antonio, TX · On-site

$71K - $145K/yr

This role is essential in protecting patient safety, ensuring highquality clinical data, and ... education, training, or completion of a CRA training program considered. * Basic knowledge of ...

CRA 1, IQVIA Biotech

Cleveland, OH · On-site

$71K - $145K/yr

This role is essential in protecting patient safety, ensuring highquality clinical data, and ... education, training, or completion of a CRA training program considered. * Basic knowledge of ...

CRA 1, IQVIA Biotech

New York, NY · On-site

$71K - $145K/yr

This role is essential in protecting patient safety, ensuring highquality clinical data, and ... education, training, or completion of a CRA training program considered. * Basic knowledge of ...

Showing results 41-60

Biotech Patient Education information

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$23

$37

How much do biotech patient education jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for biotech patient education in the United States is $23.09, according to ZipRecruiter salary data. Most workers in this role earn between $17.55 and $26.44 per hour, depending on experience, location, and employer.

What is biotech patient education?

Biotech patient education involves providing patients and their families with clear, accurate information about biotechnology-based treatments, therapies, and diagnostics. This helps patients understand how biotechnological advances may impact their care, including how to use new medications, devices, or participate in clinical trials. The goal is to empower patients to make informed decisions, improve adherence to treatment, and enhance overall health outcomes.

How does a Biotech Patient Education specialist typically collaborate with healthcare providers to improve patient understanding and outcomes?

Biotech Patient Education specialists work closely with healthcare providers, such as physicians, nurses, and pharmacists, to develop and deliver educational materials that help patients understand complex biotech treatments. They may conduct training sessions, join multidisciplinary care teams, and gather feedback from clinicians to ensure patient resources are accurate and accessible. This collaboration is crucial for addressing patient questions, improving adherence to therapy, and ultimately enhancing health outcomes. Open communication and a shared goal of patient-centered care are key components of these partnerships.

What are the key skills and qualifications needed to thrive in Biotech Patient Education, and why are they important?

To thrive in Biotech Patient Education, you need a background in life sciences or healthcare, strong communication abilities, and often a bachelor's or advanced degree in a health-related field. Familiarity with biotech products, patient education platforms, and regulatory compliance systems is typically required. Outstanding interpersonal skills, cultural sensitivity, and the ability to simplify complex information help you connect with diverse patient populations. These skills ensure patients understand their treatments and make informed decisions, leading to better health outcomes and compliance.

What is the difference between Biotech Patient Education vs Biotech Medical Writer?

AspectBiotech Patient EducationBiotech Medical Writer
Required CredentialsLife sciences degree, communication skillsLife sciences degree, writing certifications
Work EnvironmentHealthcare settings, patient-facing rolesCorporate, pharmaceutical, or biotech companies
Employer & Industry UsageHospitals, clinics, biotech firmsPharmaceutical companies, medical publishing
Common Search & Comparison IntentUnderstanding patient-focused rolesMedical writing and documentation

Biotech Patient Education focuses on creating understandable health information for patients, often working directly with healthcare providers. In contrast, Biotech Medical Writers primarily develop scientific documents, regulatory submissions, and marketing materials for industry professionals. While both roles require a background in life sciences, their audiences and daily tasks differ significantly.

What jobs can I get after studying biotechnology?

Biotech patient education professionals can pursue roles such as patient educators, medical science liaisons, clinical research coordinators, or health communication specialists. These jobs often require strong communication skills, knowledge of biological sciences, and familiarity with medical or laboratory environments.
More about Biotech Patient Education jobs

What cities are hiring for Biotech Patient Education jobs?

Cities with the most Biotech Patient Education job openings:

What states have the most Biotech Patient Education jobs?

States with the most job openings for Biotech Patient Education jobs include:

Infographic showing various Biotech Patient Education job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, and 4% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $48,028 per year, or $23.1 per hour.

CRA 1, IQVIA Biotech

IQVIA

Bloomington, IL • On-site

$71K - $145K/yr

Full-time

Re-posted 7 days ago


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 224 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.

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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