Назад
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3 дня назад

Sr Site Activation Specialist

62 800 - 157 100$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
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
Sr Site Activation Specialist (Clinical Research): Managing country-level site feasibility, identification, regulatory documentation, and activation activities for clinical studies with an accent on site coordination, document quality, and compliance with regulations and SOPs. Focus on tracking approvals and contracts, maintaining study systems, planning timelines, and solving site activation issues across project teams.

Location: Durham, North Carolina, United States of America

Salary: $62,800–$157,100 annual base pay

Company

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

What you will do

  • Act as the single point of contact for investigative sites, Site Activation Managers, project management, and internal departments.
  • Perform site feasibility, identification, start-up, and activation activities in line with regulations, SOPs, work instructions, and project requirements.
  • Prepare, review, distribute, and quality-control site documents, regulatory materials, ethics submissions, informed consent forms, and investigator packages.
  • Maintain study systems, databases, tracking tools, timelines, and project-specific information.
  • Track document approvals and execution, review site performance metrics, and implement contingency plans when needed.
  • Provide local expertise and updates to Site Activation Managers, project teams, management, and sponsors.

Requirements

  • Bachelor’s degree in life science or a related field.
  • At least 3 years of clinical research or relevant experience, or an equivalent combination of education, training, and experience.
  • At least 3 years of clinical research experience, including 1 year in a leadership capacity.
  • Knowledge of clinical study site activation, regulatory documentation, SOPs, and quality-control processes.
  • Role location: Durham, North Carolina, United States of America.

Culture & Benefits

  • Full-time employment.
  • Potential incentive plans, bonuses, and health and welfare benefits may be available in addition to base pay.
  • Equal opportunity employment practices.

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