Medical Data Review Manager – Rheumatology

IQVIA

. Review structured clinical patient data output without direct access to medical charts to ensure medical plausibility, protocol adherence, completeness, and readiness for the next level of review .

Posted 10/8/2026full-timeRemote • Argentina, BrazilMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in reviewing clinical trial data for medical plausibility and protocol adherence, with a strong background in Rheumatology and clinical research. Proficient in managing competing priorities while maintaining effective communication and relationships with stakeholders.

Highest-signal resume keywords

Rheumatology SpecializationClinical Research ExperienceSub-Investigator or Principal Investigator ExperienceAdvanced English Communication SkillsMedical Terminology Knowledge

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Data ReviewProtocol Adherence AssessmentAnomaly IdentificationLaboratory Result EvaluationAdverse Event ReviewDosing Record VerificationInclusion and Exclusion Criteria ReviewPatient Data AnalysisClinical Trial KnowledgeMedical History Review

Soft Skills

Motivational SkillsInfluencing SkillsCoaching SkillsCustomer FocusRelationship Building

Certifications & Qualifications

Rheumatology Certification

Industry Keywords

Clinical TrialsPharmaceutical CompaniesCROMedical ChartsPatient Reported DataInvestigational ProductSafety ConditionsEnd-of-Treatment DocumentationEnd-of-Study DocumentationClinical Research Site

About the role

Key responsibilities & impact

Review structured clinical patient data output without direct access to medical charts to ensure medical plausibility, protocol adherence, completeness, and readiness for the next level of review
Identify anomalies in patient-reported data requiring investigation with clinical sites
Review inclusion and exclusion criteria for clinical trial patient acceptance
Review investigational product dosing records for protocol adherence and inaccurate or missed dosages
Review Adverse Events, Concomitant Medication, and medical history information for completeness, plausibility, supporting information, and protocol adherence
Ensure end-of-treatment and end-of-study information is correctly documented
Review laboratory results for completeness, protocol schedule adherence, and potential unreported safety conditions
Review other information as necessary to determine readiness for next-level review
Interact with Medical Review staff to verify information and triage data issues or action items
Attend kick-off meetings, weekly team meetings, and client meetings as needed or requested

Requirements

What you’ll need

Specialization in Rheumatology, certified (mandatory)
Bachelor's Degree in Medicine, graduated and specialized in Rheumatology (mandatory; only physicians considered)
5 years of related experience in clinical research at research site level or CRO/Pharmaceutical companies
Experience as Sub-Investigator or Principal Investigator considered relevant
Advanced English level and strong communication skills in English
Understanding of clinical/medical data related to clinical trials
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

Benefits

Comp & perks

Home-based work arrangement
Global scope position