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3 дня назад

Associate Medical Director (Psychiatry)

Формат работы
remote (только Argentina)
Тип работы
fulltime
Грейд
middle
Английский
b2
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
Associate Medical Director (Psychiatry) (Clinical Trials): Providing medical oversight and protocol support for psychiatric clinical trials, including patient safety, eligibility decisions, adverse event review, and collaboration with investigative sites and project teams, with an accent on medical review, pharmacovigilance, and regulatory-quality documentation. Focus on evaluating serious adverse events, reviewing clinical study reports and patient narratives, supporting protocol interpretation, and addressing urgent site issues.

Location: Home-based in Argentina, with occasional international travel for meetings

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries.

What you will do

  • Act as a global, regional, or back-up Medical Advisor for assigned clinical trial projects.
  • Provide medical support to investigative sites and project staff on protocol clarifications, inclusion and exclusion decisions, patient safety, and eligibility.
  • Contribute to the medical review of protocols, Investigative Drug Brochures, Case Report Forms, clinical study reports, and patient narratives.
  • Review and clarify adverse events, including serious adverse events, in collaboration with Pharmacovigilance.
  • Provide therapeutic-area training, attend Investigator Meetings, and participate in project, kick-off, and client meetings.
  • Remain available to respond to urgent protocol-related issues at investigative sites.

Requirements

  • Medical degree from an accredited and internationally recognized medical school.
  • Specialty board certification in Psychiatry is mandatory.
  • Advanced written and spoken English is mandatory.
  • Three to five years of relevant clinical trial experience as an Investigator, Sub-Investigator, or in a related Pharma or CRO role.
  • Good communication and presentation skills in Spanish and English, plus the ability to maintain effective relationships with colleagues, managers, and clients.
  • A current and valid medical license from the country or region where the candidate resides and works is required.

Culture & Benefits

  • Home-based position with occasional international travel.
  • Opportunity to support clinical research and the development of innovative medical treatments.
  • Work across global and regional clinical trial projects with investigative sites, clients, and Pharmacovigilance teams.

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