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Location
Remote (Argentina)
Seniority
Junior · 2+ years exp
Employment
Full-Time
Overview
Company
Impact
Profile match
IQVIA is an American company formed in 2016 by the merger of the contract research organisation Quintiles, founded in 1982, with the pharmaceutical data business IMS Health. It runs clinical trials on behalf of drug and device makers and simultaneously operates one of the largest healthcare data estates in the world, covering prescriptions, claims and electronic medical records, which it sells back to the same industry for commercial planning and real-world evidence studies. Headquartered in Durham, North Carolina and listed on the New York Stock Exchange, it employs close to ninety thousand people and combines the trial and data businesses in what it calls connected intelligence.

Job Overview

Remote Research Clinical Regional Specialists (RS) are an integral part of remote visit delivery, liaising with clinical teams, clinicians, and investigator sites for remote visits. The RS works in partnership with the RRC Lead providing support with remote visit activities to mitigate risk, control cost, manage project schedule, and ensure customer satisfaction related to assigned project/s.

Essential Functions

Site and Nurse Onboarding

- Conduct outreach and training for investigator sites opting into RRC services.

- Train and onboard research clinicians, ensuring they are prepared and study-ready.

- Manage access to systems like Study Hub and Thinking Cap for both site staff and clinicians.

Remote Visit Coordination

- Receive and process Visit Request Forms (VRFs).

- Assign and confirm clinicians for remote visits.

- Coordinate visit logistics including supplies, equipment, and courier services.

- Ensure all required documentation (e.g., DOA logs, nurse credentials) is complete and uploaded.

Document and Data Management

- Maintain and update Smartsheet trackers for sites, visits, and nurses.

- Perform quality checks on source documents and ensure timely corrections.

- Review uploaded documents in Study Hub and notify relevant stakeholders.

Training and Compliance

- Deliver study-specific training to sites and clinicians.

- Ensure compliance with GCP, ICH, HIPAA, and IQVIA SOPs.

Communication and Support

- Serve as the primary liaison between sites, nurses, and internal study teams.

- Provide ongoing support and retraining to nurses as needed.

- Escalate issues to RNPS Lead and ensure resolution.

Courier and Logistics Management

- Book and track courier shipments for study drug, samples, and documents.

- Manage inventory and supply needs for nurses and depots.

Requirements

  • Bachelor's Degree Life sciences or other related field • Typically requires around 2 years of prior relevant experience on site management(Site Coordinator experience or CRA experience) - with visit coordinator skills or relevant project management experience
  • Advanced level of English is a must. All interviews will be in English.

#LI-NRJ #LI-Remote

Please, make sure to submit your CV in English. It will be assessed by a global team.

IQVIA contacts candidates exclusively through its official recruitment channels, including corporate email addresses ending in @iqvia.com and company-authorized recruitment platforms.

If you receive a suspicious communication claiming to be from IQVIA through unofficial channels, we recommend that you do not share any personal information and contact us through our official channels for verification.

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.

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