Remote Site Research Assistant (Santa Fe)

Job Overview

Perform a variety of administrative and operational tasks to support clinical trials and assist with clinical procedures required to collect data from patients enrolled or being considered for enrollment in research studies.

Essential Functions

• Provide clinical research support to investigators and site staff.

• Verify and correct study information on source documents; resolve queries and discrepancies; provide feedback to site personnel.

• Enter study data into the EDC system, ensuring accuracy, completeness, and quality control.

• Prepare, organize, and maintain study files; compile and submit required documentation within established timelines.

• Collect and submit regulatory and ethics documents related to the study.

• Maintain the FDA 1572 for assigned studies.

• Schedule subject visits and prepare necessary reports and documents prior to each visit.

• Enter visit data into the CTMS to track patient visits and completed procedures against the study budget.

Qualifications

• High School Diploma or equivalent required.

• Availability to work based in Santa Fe - Argentina (100% remote)

• Availability to work part-time (20 hours per week)

• Availability to work in a fixed term contract

• Educational equivalent plus 2 years of relevant experience in a clinical or medical setting, or a combination of education, training, and experience.

• Basic understanding of clinical trial processes.

• Strong knowledge of departmental, protocol, and study‑specific procedures, consent forms, and visit schedules.

• Basic knowledge of medical terminology.

• Proficiency with MS Windows and Office applications (Access, Outlook, Excel, Word).

• Excellent interpersonal and communication skills.

• Strong attention to detail.

• Ability to build and maintain effective working relationships with colleagues, managers, and clients.

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

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.