Uro-Oncology Key Account Manager TX-NM

Clinical Research Associate I (CRA I) – Oncology Solid Tumor IQVIA Biotech is now hiring for CRA I with a minimum of 6 months of on‑site monitoring. Experience monitoring in oncology solid tumor is required. 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. 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 high‑quality clinical data, and maintaining study integrity. Key Responsibilities 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. Verify that study activities are performed according to regulatory requirements and sponsor expectations, escalating quality concerns as necessary. 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). Build and maintain strong communication with investigative sites, providing protocol training, setting expectations, addressing site‑level challenges, and supporting recruitment planning to help sites meet enrollment targets. 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. Prepare detailed monitoring visit reports, follow‑up letters, and all required study documentation to ensure audit readiness and transparent oversight. Manage multiple tasks, prioritize effectively, and work independently while maintaining productive team relationships. Qualifications Bachelor’s degree required; a scientific or healthcare discipline is preferred. 6 months to 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. Potential Base Pay Range $71,900.00 – $119,900.00 annualized. Actual base pay offered may vary based on factors such as qualifications, location, and schedule. Incentive plans, bonuses, and additional compensation may be offered along with a range of health and welfare benefits. Equal Opportunity Employer 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. Integrity Statement 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. #J-18808-Ljbffr