Medical Data Review Manager – Rheumatology

🔥 59 minutes ago

🌐 Argentina, Brazil – Remote

🇦🇷 Argentina – Remote 🇧🇷 Brazil – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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IQVIA

WebsiteLinkedInAll Job Openings

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 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

• 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

• Home-based work arrangement • Global scope position