Senior Clinical Research Associate, Early Clinical Development

divh2Senior CRA 1/h2pIQVIA Early Clinical Development is hiring for a Senior CRA 1. Ideal candidates will have Phase 1 experience across a variety of therapeutics. Seeking candidates located Central or West Coast, US./ppJob 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./ppKey Responsibilities/pulliConduct all types of site visitsselection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines./liliCollaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals./liliDeliver protocol and study-specific training to site personnel and maintain consistent communication to manage expectations and resolve issues./liliAssess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity./liliMonitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution of data queries./liliEnsure 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./liliDocument site management activities, visit outcomes, and follow-up actions through detailed reports and correspondence./liliWork closely with cross-functional project teams to support study execution and ensure alignment with project goals./liliDepending on the project, you may also support site-level recruitment planning and financial management, including invoice collection and budget tracking./li/ulpQualifications/pulliBachelors degree in life sciences or health-related field (or equivalent experience)./liliRequires at least 1.5 years of on-site monitoring experience./liliStrong understanding of GCP, ICH guidelines, and regulatory requirements./liliAbility to travel as required by the project./li/ulpIQVIA 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./ppIQVIA 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./ppIQVIA 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./ppThe potential base pay range for this role, when annualized, is $87,200.00 - $169,300.00. 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./p/div