Medical Data Reviewer Job at IQVIA – Remote Nephrologist Role
The medical data reviewer job opportunity at IQVIA offers licensed nephrologists a chance to work in a fully remote environment while contributing to clinical research and patient safety. This remote job for doctors allows professionals to review clinical patient data, ensure protocol adherence, and support the accuracy of medical information used in clinical trials. For professionals exploring work-from-home medical jobs and IQVIA careers, this role based in Buenos Aires provides an excellent opportunity within the growing landscape of medical jobs in South America.
Job Details:
- Job Title: Nephrologist – Medical Data Review Manager
- Location: Buenos Aires, Argentina
- Employment Type: Full-time, 100% home-based role
- Job Id: R1530381
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. Professionals interested in IQVIA careers, remote jobs for doctors, and medical jobs in South America can explore more opportunities through the company’s career platform.
Job Description:
This medical data reviewer job is a full-time, 100% home-based role designed for nephrologists with clinical experience. The position focuses on reviewing structured clinical patient data output without direct access to medical charts to ensure medical plausibility and determine adherence to protocol and overall completeness and readiness of the supplied patient information for next level of review.
This role is ideal for professionals seeking work from home medical jobs and remote jobs for doctors while contributing to clinical research and patient safety initiatives.
Qualifications:
- Licensed Nephrologist 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.
- 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 the 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 the 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 the 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.
