Назад
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2 дня назад

Associate Site Activation Manager

60 300 - 157 100$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
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
Associate Site Activation Manager (Clinical Research): Directing and managing site identification, selection, regulatory processes, contracting, and activation for assigned clinical studies across at least one region with multiple countries with an accent on regulatory strategy, study start-up delivery, and project oversight. Focus on accelerating site activation, resolving cross-country operational challenges, maintaining approvals and essential documents, and coordinating internal and external stakeholders.

Location: Durham, North Carolina, United States of America

Annual base pay: $60,300–$157,100

Company

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

What you will do

  • Direct strategic, operational, and financial delivery of site activation activities, including site identification, selection, ethics and regulatory processes, and site contracting.
  • Plan and oversee study start-up from pre-award through site activation and lifecycle maintenance across at least one region with multiple countries.
  • Develop and maintain Site Activation Management Plans, project plans, timelines, tracking tools, and internal systems.
  • Define regulatory strategies, assess regulatory complexity, and support submissions, approvals, authorizations, and contract negotiations.
  • Collaborate with internal and external stakeholders, provide project updates, resolve issues, and maintain customer relationships.
  • Create or review study documentation and deliver presentations or training to clients, colleagues, and professional bodies.

Requirements

  • Bachelor’s degree in life science or a related field.
  • At least 3 years of relevant experience in a scientific or clinical environment.
  • Demonstrable experience in an international role, or an equivalent combination of education, training, and experience.
  • In-depth knowledge of clinical systems, procedures, corporate standards, medical terminology, clinical research, and regulations.
  • Strong communication, organization, interpersonal, prioritization, delegation, and multitasking skills.
  • Proficiency with Microsoft Office and email applications, with strong attention to detail.

Culture & Benefits

  • Work supports the development and commercialization of medical treatments and improved patient outcomes.
  • Equal opportunity employment is provided.
  • Health, welfare, and other benefits may be available.
  • Additional incentive plans, bonuses, or other compensation may be offered depending on the position.

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