Clinical Research Associate, Sponsor Dedicated

Clinical Research Associate, Sponsor Dedicated

Liverpool, United States of America | Full time | Field-based | Job  R1541733

To be eligible for this position, you must reside in the same country where the job is located.

• 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 plan in line with project needs to enhance predictability.
• Administer protocol and related study training to assigned sites and maintain regular communication to manage 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; report quality issues as appropriate.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and resolution of data queries; may support start‑up phase.
• Ensure required site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator’s Site File (ISF) is maintained per GCP and local regulatory requirements.
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting visit reports, follow‑up letters and other required study documentation.
• Collaborate and liaise with study team members for project execution support as appropriate.
• When applicable, support development of a project subject recruitment plan at the site level.
• When applicable, manage site financial matters according to clinical trial agreement and retrieve invoices per local requirement.

• Bachelor’s Degree in a scientific discipline or health care; an equivalent combination of education, training and experience may be accepted.
• At least two years of on‑site monitoring experience.
• Good knowledge of and application of applicable clinical research regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Good therapeutic and protocol knowledge provided in company training.
• Computer proficiency in Microsoft Word, Excel, PowerPoint and use of laptop and/or mobile devices as applicable.
• Strong written and verbal communication skills with a 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.

Potential base pay range: $71,900.00 – $ (annualized). Actual base pay may vary based on job‑related qualifications, location and schedule. Incentive plans, bonuses and other compensation may be offered, in addition to a range of health and welfare benefits.

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.

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.