Clinical Research Associate, Sponsor Dedicated

Clinical Research Associate, Sponsor Dedicated Elk Grove, United States of America | Full time | Field-based | R1541733 To be eligible for this position, you must reside in the same country where the job is located. Essential Functions Perform site monitoring visits (selection, initiation, monitoring and close‑out) in accordance with contracted scope of work and Good Clinical Practice. Work with sites to adapt, drive, and track subject recruitment plans in line with project needs to enhance predictability. Administer protocol and related study training to assigned sites and establish regular lines of communication to manage ongoing project expectations and issues. Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations; Escalate quality issues as appropriate. Manage progress of assigned studies by tracking regulatory submissions and approvals, recruitment/enrollment, case report form completion and submission, and data query generation and resolution; may support start‑up phase. Ensure copies/originals of site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator’s Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management, monitoring visit findings, and action plans by submitting regular visit reports, generating follow‑up letters and other required study documentation. Collaborate and liaise with study team members for project execution support as appropriate. Accountable for supporting development of project subject recruitment plans on a per‑site basis, if applicable. Accountable for site financial management per the executed clinical trial agreement and retrieve invoices according to local requirements, if applicable. Qualifications Bachelor’s Degree in a scientific discipline or health care preferred. At least 2 years of on‑site monitoring experience. Equivalent combination of education, training and experience may be accepted in lieu of degree. Good knowledge of and skill in applying applicable clinical research regulatory requirements (e.g., GCP and ICH guidelines). Good therapeutic and protocol knowledge as provided in company training. Computer skills including proficiency in Microsoft Word, Excel, PowerPoint and use of laptop/iPhone/iPad platforms, where applicable. Written and verbal communication skills including good command of English. Organizational and problem‑solving skills. Effective time and financial management skills. Ability to establish and maintain effective working relationships with coworkers, managers, and clients. Compensation The potential base pay range for this role, when annualized, is $71,900.00 – $189,000.00. Incentive plans, bonuses, and other forms of compensation may be offered in addition to health and welfare benefits. EEO Statement 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