Назад
Company hidden
6 дней назад

Clinical Project Sppt Spec (COA/eCOA)

Формат работы
remote (только Brazil)
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
Brazil
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:
/
TL;DR
Clinical Project Sppt Spec (COA/eCOA): Leading end-to-end COA and eCOA licensing services for global clinical studies with an accent on client delivery, compliance, and technology-enabled managed services. Focus on coordinating complex licensing activities, mentoring delivery consultants, managing risks and timelines, and supporting proposals, financial tracking, and product improvements.

Location: São Paulo, Brazil; remote-friendly

Company

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

What you will do

  • Lead end-to-end COA and eCOA licensing services across client engagements and clinical studies.
  • Manage license identification, permissions, fee negotiation coordination, contract execution support, and ongoing study support.
  • Coordinate Associate Delivery Consultants and Delivery Consultants, including prioritization, issue resolution, mentoring, and knowledge sharing.
  • Manage project timelines, costs, risks, vendor dependencies, and mitigation plans.
  • Support licensing estimates, proposals, invoicing coordination, revenue tracking, sales activities, and client presentations.
  • Provide client feedback to product management, clinical outcomes, and professional services teams to improve processes and tools.

Requirements

  • Bachelor’s degree in Computer Science, Life Sciences, Clinical Research, a related field, or equivalent relevant experience.
  • Experience with COA and/or eCOA licensing, clinical study support, or related managed services delivery.
  • Familiarity with eCOA platforms and clinical trial technology implementations.
  • Experience in CRO, life sciences, healthcare, or pharmaceutical development environments.
  • Experience leading complex client engagements or projects with limited supervision.
  • Strong understanding of quality, compliance, documentation, problem-solving, organization, and client-facing communication.

Culture & Benefits

  • Flexible, remote-friendly work environment.
  • Opportunity to mentor and develop a delivery team.
  • Work on global clinical studies supporting the development of medical treatments.
  • Exposure to technology, clinical outcomes, client delivery, product improvement, and commercial growth.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →