Remote Medical Data Review Manager — Rheumatology

IQVIA Inc; Municipio de Esquel; Remote; ARS 136,430,000 - 204,645,000; Full time

Job summary

IQVIA is seeking a Medical Data Review Manager for a remote, global position. Requires a medical degree with rheumatology specialization and 5+ years in clinical research. The role focuses on data plausibility, protocol adherence, and readiness for further review across time zones.

Engagement includes collaboration with medical review staff, attending kick-off and team meetings, and ensuring data integrity throughout the trial lifecycle.

Qualifications

• Must hold a medical degree with rheumatology specialization.
• At least 5 years in clinical research at site, CRO, or pharma.
• Advanced English and global communication.
• Strong understanding of clinical/medical data.
• Background in Medical Terminology, Pharmacology, Anatomy, and Physiology.
• Excellent motivational, influencing and coaching skills.
• Ability to manage multiple projects and priorities.
• Strong customer focus and relationship skills.

Responsibilities

• Identify anomalies in patient data requiring site follow-up.
• Review inclusion/exclusion criteria for trial eligibility.
• Audit dosing records for protocol adherence and accuracy.
• Assess adverse events, concomitant meds, and medical history for data integrity.
• Verify end-of-treatment and end-of-study documentation.
• Review laboratory results for completeness and safety signals.
• Evaluate other information to determine overall readiness for review.
• Collaborate with medical review staff and escalate issues.
• Attend kick-off, weekly, and client meetings as needed.

Skills

Advanced English

Education

Bachelor's Degree in Medicine, specialized in Rehumatology

Job description

IQVIA is seeking a Medical Data Review Manager for a remote, global position. Requires a medical degree with rheumatology specialization and 5+ years in clinical research. The role focuses on data plausibility, protocol adherence, and readiness for further review across time zones.

Engagement includes collaboration with medical review staff, attending kick-off and team meetings, and ensuring data integrity throughout the trial lifecycle.