The Clinical Research Associate will monitor and manage clinical trial sites to ensure strict adherence to study protocols, GCP/ICH guidelines, and regulatory requirements. Responsibilities include conducting site visits, overseeing recruitment plans, managing documentation, and providing training to site staff.
Join our dynamic team as a Clinical Research Associate! You’ll play a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study protocols, regulations, and sponsor requirements. Be at the forefront of groundbreaking cancer research and make a real impact on patients’ lives.
Ensure all site documents are filed in the Trial Master File (TMF) and Investigator’s Site File (ISF) per GCP/ICH and local regulations.
Generate visit reports, follow-up letters, and other necessary documentation.
Mentor clinical staff through co-monitoring and training visits.
Work closely with study team members to support project execution.
Education: BS degree required; a degree in a scientific discipline or healthcare is preferred.
3+ years of on site oncology monitoring experience strongly preferred. 1.5+ years of oncology monitoring experience can be considered. Phase 1 oncology experience is required.
Proficient in GCP and ICH guidelines. Strong therapeutic and protocol knowledge in Phase 1 oncology trials. Excellent computer skills, including Microsoft Office and mobile devices. Effective communication, organizational, and problem-solving abilities. Strong time management skills. Ability to build and maintain effective working relationships.
Why Join Us? Be part of a team that’s pushing the boundaries of cancer research. You’ll have the opportunity to work on cutting-edge Phase 1 oncology trials, collaborate with top professionals in the field, and contribute to life-changing advancements in cancer treatment. If you’re passionate about making a difference and have the expertise we’re looking for, we’d love to hear from you!
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 [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 [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 - $189,000.00. 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.
Candidates must hold a bachelor's degree in a scientific or healthcare discipline and possess at least 1.5 to 3 years of oncology monitoring experience. Proficiency in Phase 1 oncology trials and strong knowledge of GCP/ICH regulatory standards are required.
Market context
California sponsor-aligned oncology CRA roles are often in demand because trial activity is concentrated in major research hubs and employers look for monitors who can work independently across complex studies. This role is competitive because it requires oncology Phase 1 monitoring experience, GCP/ICH knowledge, and a scientific or healthcare degree. Review the AI-summarized requirements and benefits here to save time, then tailor your application to specific oncology protocols and monitoring experience.
