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3 часа назад

In-House Clinical Research Associate II (Medtech)

Формат работы
remote (только Europe)
Тип работы
fulltime
Грейд
middle
Английский
c1
Страна
Argentina/Chile/Mexico +3 еще
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
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TL;DR

In-House Clinical Research Associate II (Medtech): Supporting clinical study sites and project teams by managing essential documentation, tracking milestones, and ensuring regulatory compliance with an accent on ICH-GCP standards. Focus on maintaining trial master files, facilitating site communication, and coordinating clinical system data to ensure study integrity across the LATAM region.

Location: Must be based in Mexico, Brazil, Argentina, Colombia, Chile, or Peru

Company

hirify.global is a global organization providing specialized services to the life sciences industry to accelerate the development of new therapies.

What you will do

  • Assist with investigator recruitment and site feasibility activities.
  • Maintain and distribute Investigator Site Files and ensure data accuracy in the Trial Master File (TMF).
  • Act as the primary point of contact for study sites, addressing management issues and supply logistics.
  • Track study milestones and activities using the Clinical Trial Management System (CTMS).
  • Ensure timely data entry by sites in EDC systems and facilitate database closure procedures.
  • Support CRA activities and regulatory submissions in compliance with ICH-GCP guidelines.

Requirements

  • Must be based in Mexico, Brazil, Argentina, Colombia, Chile, or Peru.
  • Bachelor's degree or international equivalent in a scientific or healthcare discipline.
  • Minimum of 2 years of relevant clinical research experience.
  • Fluency in English communication, both verbal and written.
  • Proficiency in Microsoft Office (Outlook, Word, Excel, PowerPoint).
  • Working knowledge of the drug development process and ICH-GCP regulations.

Culture & Benefits

  • Opportunity to build the foundation of a new regional function in LATAM.
  • Professional development through mentorship and independent project work.
  • Collaborative environment focused on precision and clinical excellence.
  • Supportive remote work culture with clear adherence to global regulatory standards.

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