## About IQVIA Biotech

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. As a leading global provider of clinical research services, commercial insights, and healthcare intelligence, we create intelligent connections to accelerate the development and commercialization of innovative medical treatments.

## The Role

We're hiring a Clinical Research Associate I (CRA I) to play a key role in supporting the successful conduct of clinical research studies. In this position, you'll be responsible for site monitoring and site management activities, ensuring that assigned study sites conduct trials in full 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.

You must have a minimum of 6 months of on-site monitoring experience and specific experience monitoring in oncology solid tumor studies.

## What You'll Do

As a CRA I, you'll 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'll verify that study activities are performed according to regulatory requirements and sponsor expectations, escalating quality concerns as necessary.

During these visits, you'll 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). Building and maintaining strong communication with investigative sites is a central part of this role. You'll provide protocol training, set expectations, address site-level challenges, and support recruitment planning to help sites meet enrollment targets.

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

## What We're Looking For

You'll need a Bachelor's degree; a scientific or healthcare discipline is preferred. The position requires 6 months to 2 years of relevant experience, with equivalent combinations of education, training, or completion of a CRA training program also considered.

Basic knowledge of clinical research regulations (GCP/ICH) is required, and you must have the ability to travel as required by the project.

## Compensation and Benefits

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 factors including job-related qualifications such as knowledge, skills, education, and experience; location; and schedule. Dependent on the position offered, incentive plans, bonuses, and other forms of compensation may be offered in addition to a range of health and welfare and other benefits.

## Our Commitment

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. We seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.