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3 дня назад

Medical Data Review Manager (Rehumatology)

Формат работы
remote (только Argentina)
Тип работы
fulltime
Английский
c1
Страна
Argentina
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Medical Data Review Manager (Rehumatology): Reviewing structured clinical patient data for medical plausibility, protocol adherence, completeness, and readiness for further review with an accent on clinical trial eligibility, dosing records, adverse events, laboratory results, and treatment outcomes. Focus on identifying anomalies, assessing patient safety signals, and coordinating data issue triage across medical review teams and clinical stakeholders.

Location: Buenos Aires, Argentina; home-based role with global scope

Company

hirify.global 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.
  • Assess inclusion and exclusion criteria, investigational product dosing, adverse events, concomitant medications, and medical history.
  • Review end-of-treatment, end-of-study, and laboratory information, including potential safety conditions not reported as adverse events.
  • Collaborate with medical review staff to triage new data issues and previously identified action items.
  • Attend kick-off, weekly team, and client meetings as needed.

Requirements

  • Completed medical degree and mandatory specialization in Rheumatology; only physicians will be considered.
  • At least 5 years of relevant 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 for a global-scope role.
  • Understanding of clinical and medical data in clinical trials, including medical terminology, pharmacology, anatomy, and physiology.
  • Ability to manage multiple projects, competing priorities, stakeholder relationships, and customer-focused collaboration.

Culture & Benefits

  • Home-based work arrangement.
  • Global-scope collaboration with medical review staff, clinical sites, clients, and cross-functional stakeholders.
  • Participation in regular team and client meetings.

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