Site Research Assistant (CABA)

Posted Yesterday
Be an Early Applicant
Buenos Aires, Ciudad Autónoma de Buenos Aires, ARG
In-Office
Junior
Healthtech
The Role
Support clinical trials by performing administrative and clinical tasks: verify source documents, enter and quality-check data in EDC, maintain study and regulatory files (including FDA 1572), schedule subject visits, track visits in CTMS, and compile/submit study documentation on time while working with investigators and site staff.
Summary Generated by Built In

Job Overview
Perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies.
Essential Functions
• Provide clinical research support to investigators and site staff, including
• Verify and/or correct research study information on source documents; research queries and variances; and provide
feedback to the site data collector.
• Input research study data into trial Electronic Data Capture (EDC) system, maintaining quality control for content,
accuracy, and completeness.
• Prepare and maintain research study files. Compile, collate and submit study information within established deadlines.
• Collect and submit regulatory/ethics documentation pertaining to the research study.
• Maintain the FDA 1572 form for assigned research studies.
• Schedule subject visits and generate appropriate reports and documents for research subjects prior to visits.
• Input visit data into clinical trial management system (CTMS) to track patient visits and procedures completed against the study budget.
Qualifications
• Bachelor degree
• Educational equivalent and 2 years’ relevant work experience in a clinical environment or medical setting; or equivalent combination of education, training and experience Req
• Basic knowledge of clinical trials
• In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study
schedules
• Basic knowledge of medical terminology
• Basic skill in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
• Excellent interpersonal skills
• Ability to pay close attention to detail
• Ability to establish and maintain effective working relationships with coworkers, 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.

Skills Required

  • Bachelor degree
  • Educational equivalent and 2 years' relevant work experience in a clinical environment or equivalent combination of education, training and experience
  • Basic knowledge of clinical trials
  • In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
  • Basic knowledge of medical terminology
  • Basic skill in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
  • Excellent interpersonal skills
  • Ability to pay close attention to detail
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients

IQVIA Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about IQVIA and has not been reviewed or approved by IQVIA.

  • Healthcare Strength Healthcare coverage is positioned as comprehensive, spanning medical/dental/vision plus programs like telemedicine, EAP resources, and additional insurance options. Feedback suggests the health offering is a meaningful part of the overall rewards package, though details can vary by location and plan design.
  • Retirement Support Retirement benefits include an employer match structure that supports employee contributions through a defined formula. This adds steady long-term value to total rewards beyond base salary.
  • Leave & Time Off Breadth Time off offerings include vacation/paid time off, holidays, and flexibility themes, with some roles described as having discretionary or unlimited time-off models. This can make the package feel more attractive even when cash compensation is viewed as only mid-range.

IQVIA Insights

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The Company
Bangalore, Karnataka
61,500 Employees
Year Founded: 2016

What We Do

IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 70,000 employees, IQVIA conducts operations in more than 100 countries. To learn more, visit www.iqvia.com.

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