CRA 2, Oncology, IQVIA Biotech

IQVIA; Durham (NC); On-site; USD 75,000 - 175,000; Full time

Job summary

IQVIA Biotech in Durham, NC seeks a Clinical Research Associate (CRA) II to monitor sites and ensure protocol adherence, regulatory compliance, and data integrity across oncology trials.

This on-site role requires at least 1 year of monitoring experience, a life sciences degree, and willingness to travel. You will train site staff, manage site communications, and help maintain trial documentation and TMF quality.

Qualifications

• At least 1 year of on-site monitoring experience.
• Strong knowledge of GCP, ICH guidelines and regulatory requirements.
• Willingness to travel as required by projects.
• Bachelor’s degree in life sciences or health-related field (or equivalent).

Responsibilities

• Conduct site visits—selection, initiation, monitoring, and close-out per scope, GCP and ICH guidelines.
• Collaborate with site staff to implement subject recruitment strategies aligned with timelines.
• Deliver protocol and study-specific training to site personnel and maintain communication to manage expectations.
• Assess site performance and adherence to protocol; escalate quality concerns as needed.
• Monitor study progress by tracking regulatory submissions, enrollment, CRFs, and data queries.
• Ensure essential documents are maintained in TMF and ISF per regulatory standards.
• Document site management activities and follow-up actions with detailed reports and correspondence.
• Work with cross-functional teams to support study execution and project goals.
• Support site-level recruitment planning and financial management when applicable.

Skills

On-site monitoring

GCP/ICH knowledge

Travel readiness

Education

Bachelor’s degree in life sciences or health-related field

Job description

IQVIA Biotech is expanding our Clinical Monitoring team and is seeking CRA 2 professionals with a minimum of 1 year of on-site monitoring experience and oncology solid tumor monitoring experience.

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

We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials. In this position, you will be responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. Your work will directly contribute to the integrity and quality of clinical research data.

Key Responsibilities

• Conduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines.
• Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals.
• Deliver protocol and study-specific training to site personnel and maintain consistent communication to manage expectations and resolve issues.
• Assess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity.
• Monitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution of data queries.
• Ensure that essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File (ISF) in accordance with regulatory standards.
• Document site management activities, visit outcomes, and follow-up actions through detailed reports and correspondence.
• Work closely with cross-functional project teams to support study execution and ensure alignment with project goals.
• Depending on the project, you may also support site-level recruitment planning and financial management, including invoice collection and budget tracking.

Qualifications

• Bachelor’s degree in life sciences or health-related field (or equivalent experience).
• Requires at least 1 year of on-site monitoring experience.
• Strong understanding of GCP, ICH guidelines, and regulatory requirements.
• 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 $74,500.00 - $175,100.00. 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.