Medical Data Review Manager – Rehumatology

🔥 13 hours ago

🌐 Argentina, Brazil – Remote

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⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

👻 Ghost score 10%

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Logo of IQVIA

IQVIA

10,000+ employees

💼 Consulting

🏭 Manufacturing

📣 Marketing

💰 $1G Post-IPO Debt on 2023-05

Consulting • Manufacturing • Marketing

IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.

📋 Description

• Review structured clinical patient data output without direct access to medical charts • 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 eligibility • Review investigational product dosing records for protocol adherence and inaccurate or missed dosages • Review Adverse Events, Concomitant Medication, and medical history information • Verify implausible data and assess impacts on other patient-reported or observed information • Ensure end-of-treatment and end-of-study information is correctly documented • Review laboratory results for completeness, protocol adherence, and potential unreported safety conditions • Review other information as needed to determine patient-information readiness • Interact with Medical Review staff to verify information and triage data issues or action items • Attend kick-off, weekly team, and client meetings as needed

🎯 Requirements

• Bachelor's Degree in Medicine, graduated and specialized in Rehumatology (mandatory; only physicians considered) • Rehumatology specialization must be certified • 5 years of related experience in clinical research at a research site, CRO, or pharmaceutical company • Experience as Sub-Investigator or Principal Investigator is 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

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