5 дней назад
Medical Data Review Manager Rheumatology
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Medical Data Review Manager Rheumatology (Clinical Trials): Reviewing structured clinical patient data for medical plausibility, protocol adherence, completeness, and readiness for further review with an accent on rheumatology expertise and patient safety assessment. Focus on identifying data anomalies, evaluating inclusion and exclusion criteria, reviewing dosing, adverse events, laboratory results, and end-of-treatment documentation, and coordinating issue resolution with medical review staff and clinical stakeholders.
Location: Home-based role in Buenos Aires, Argentina; global scope.
Company
provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Review structured clinical patient data for medical plausibility, completeness, protocol adherence, and readiness for the next level of review.
- Identify anomalies and coordinate follow-up with clinical sites to verify patient data accuracy.
- Evaluate inclusion and exclusion criteria, investigational product dosing, adverse events, concomitant medications, and medical history.
- Review laboratory results and treatment or study completion information to identify safety conditions and confirm the primary reason for treatment or study termination.
- Collaborate with medical review staff to triage new data issues and resolve previously identified action items.
- Participate in kick-off, weekly team, and client meetings as needed.
Requirements
- Completed Bachelor's Degree in Medicine with mandatory specialization and certification in Rheumatology; only physicians will be considered.
- At least 5 years of clinical research experience at a research site, CRO, or pharmaceutical company.
- Experience as a Sub-Investigator or Principal Investigator is relevant.
- Advanced English proficiency and strong communication skills are required for the global scope of the role.
- Knowledge of clinical trial data, medical terminology, pharmacology, anatomy, and physiology.
- Ability to manage multiple projects, competing priorities, stakeholder relationships, and client-focused communication.
Culture & Benefits
- Home-based work arrangement.
- Global scope and collaboration with medical review staff, clinical sites, and clients.
- Opportunities to participate in cross-functional clinical research meetings.
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