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Senior Site Activation Specialist, Informed Consent Form LEAD (Clinical Research)

Формат работы
hybrid
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
Serbia/Bulgaria/SA
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
Senior Site Activation Specialist, Informed Consent Form LEAD (Clinical Research): Leading the development, review, and rollout of informed consent forms across multiple countries and studies with an accent on protocol alignment, regulatory compliance, and timely approvals. Focus on coordinating master and country-level documents, managing regulatory updates, and resolving complex ICF-related issues with global and country teams.

Location: Hybrid; Bulgaria, South Africa, or Serbia

Company

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

What you will do

  • Lead and support the development of master and country-level Informed Consent Forms.
  • Review ICFs for accuracy, protocol alignment, and compliance.
  • Coordinate document updates resulting from regulatory or guideline changes.
  • Track approvals and ensure timely execution of ICF documentation.
  • Collaborate with sponsors and internal teams on project timelines.
  • Support and mentor country CSA specialists and act as an escalation point for ICF-related matters.

Requirements

  • Bachelor’s degree in Life Sciences or a related field.
  • At least 3 years of experience in Life Sciences.
  • Knowledge of ICH/GCP and regulatory requirements.
  • Strong communication, negotiation, and problem-solving skills.
  • Ability to manage multiple projects.

Culture & Benefits

  • Work across 21 therapeutic areas.
  • Global exposure across 141 locations.
  • Access to innovative technologies.
  • Collaborative environment focused on professional growth.

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