Work From Home Rheumatologist Job at IQVIA | Apply Now
The demand for remote jobs for doctors is rapidly increasing as healthcare organizations adopt digital clinical research models. One such opportunity is the rheumatologist job offered by IQVIA, a global leader in clinical research and healthcare intelligence. This work-from-home medical job allows licensed rheumatologists to review structured clinical patient data while contributing to clinical trial quality and patient safety. Professionals looking for IQVIA careers and medical jobs in South America can benefit from this flexible, home-based role.
Job Details:
- Job Position: Rheumatologist – Medical Data Review Manager
- Location: Buenos Aires, Argentina (Home-based)
- Job ID: R1533012
About the Company
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. The organization creates intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
As one of the growing IQVIA careers, this role contributes to clinical research quality while supporting the growing trend of remote jobs for doctors and work from home medical jobs across global healthcare organizations.
Job Description
The rheumatologist job is a full-time, 100% home-based role responsible for reviewing structured clinical patient data output without direct access to medical charts. The objective is to ensure medical plausibility, determine adherence to protocol, and evaluate the overall completeness and readiness of the supplied patient information for the next level of review.
This opportunity is ideal for physicians seeking medical jobs in South America that combine clinical expertise with clinical research data review in a flexible remote setting.
Qualifications
- Licensed Rheumatologist with clinical experience.
- Previous experience as a Sub‑Investigator or Principal Investigator (PI) will be highly valued.
- Previous clinical experience.
- English Advanced, mandatory.
- Understanding of clinical/medical data.
- Background in Medical Terminology, Pharmacology, Anatomy, and Physiology.
- Excellent motivational, influencing and coaching skills.
- Ability to work on multiple projects and manage competing priorities.
- Strong customer focus skills.
- Ability to establish and maintain effective working relationships with coworkers, managers and clients.
Key Responsibilities
- Identify any anomalies in patient reported data that require further investigation with the clinical site to determine overall accuracy.
- Review all inclusion and exclusion criteria to ensure each patient meets minimum level of acceptance into the clinical trial.
- Review investigation product dosing records to determine adherence to protocol and identify possible inaccurate / missed dosages.
- Review all reported Adverse Events (AEs), Concomitant Medication and medical history information to ensure all supporting information is expected and/or implausible data is verified and adherence to protocol expectations and its impact on other patient reported/observed information (e.g., laboratory results, AEs, etc.).
- Ensure end-of-treatment (EOT) and end-of-study (EOS) information is correctly documented to determine primary reason for the patient ending treatment or ending participation in the clinical trial.
- Review all laboratory results to ensure completeness of information and adherence to protocol schedule of events and determine if reported laboratory values represent a potential safety condition not reported in the AE information for the patient.
- Review any other information as necessary to determine overall readiness of the patient information for next level review.
- Interaction with other Medical review staff to verify information and/or triage new data issues or prior identified action items.
- Attend Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested.
