Remote Medical Data Review Lead | Global Rheumatology

Iqvia Argentina

Quilmes

Remote

ARS 1,000,000 - 1,600,000

Full time

4 days ago
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Job summary

IQVIA in Argentina is seeking a Medical Data Review Manager (Rheumatology) to lead data quality reviews for global clinical trials from a home-based position. The role focuses on ensuring medical plausibility, protocol adherence, and complete patient information for next review steps.

You will supervise data review activities, coordinate with site staff and other medical reviewers, and participate in kick-offs and client meetings.

Qualifications

  • Bachelor's Degree in Medicine, with Rheumatology specialization (mandatory).
  • At least 5 years of clinical research experience at site, CRO, or pharma. PI/Sub-Investigator background preferred.
  • Advanced English with excellent communication skills.
  • Ability to manage multiple projects and prioritize effectively.

Responsibilities

  • Identify anomalies in patient data requiring site follow-up to determine accuracy.
  • Review inclusion/exclusion criteria to ensure patients meet trial entry requirements.
  • Review dosing records to ensure adherence to protocol and detect discrepancies.
  • Review adverse events, concomitant medications, and medical history for consistency with protocol.
  • Ensure EOT/EOS data are documented to explain reasons for treatment/participation termination.
  • Review laboratory results for completeness and safety signals per protocol schedule.
  • Coordinate with medical review staff and participate in meetings as needed.

Skills

Advanced English
Coaching skills
Multi-project management
Strong customer focus

Education

Bachelor's Degree in Medicine

Job description

IQVIA in Argentina is seeking a Medical Data Review Manager (Rheumatology) to lead data quality reviews for global clinical trials from a home-based position. The role focuses on ensuring medical plausibility, protocol adherence, and complete patient information for next review steps.

You will supervise data review activities, coordinate with site staff and other medical reviewers, and participate in kick-offs and client meetings.

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