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Manager, Project Services (Clinical Research)

Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
c1
Страна
Argentina
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
Manager, Project Services (Clinical Research): Leading client delivery teams and clinical trial project management services with an accent on people development, regulatory compliance, and cross-functional coordination. Focus on executing complex Phase I-IV studies, resolving stakeholder issues, and monitoring delivery against contractual commitments and project objectives.

Location: Buenos Aires, Argentina

Company

hirify.global provides clinical research services, healthcare intelligence, and life sciences solutions that support the development and commercialization of medical treatments.

What you will do

  • Lead the day-to-day activities of the Client Delivery Team and oversee consistent, high-quality project management services.
  • Mentor and develop staff, assign work, manage performance, and support professional development.
  • Assess project management capabilities and implement improvements to service delivery processes.
  • Resolve client and operational issues, coordinate actions, and communicate outcomes to internal and external stakeholders.
  • Ensure clinical studies follow FDA, ICH, EMEA, and Good Clinical Practice requirements.
  • Coordinate cross-functional work with internal departments, vendors, sponsors, and other stakeholders across the project lifecycle.

Requirements

  • Bachelor’s degree in Life Sciences or a related field is preferred; equivalent education, training, and experience may be accepted.
  • At least 4 years of experience in clinical trials, hospital-funded research, project management, or a laboratory environment.
  • Advanced English proficiency is required, and the CV must be submitted in English.
  • Strong people management, communication, organization, problem-solving, stakeholder management, and client management skills.
  • Working knowledge of FDA, ICH, EMEA, and Good Clinical Practice requirements.
  • Experience with Microsoft Office and centralized laboratory or comparable company systems.

Nice to have

  • Direct line management experience.
  • Knowledge of Project Services or central laboratory processes.
  • Experience leading large, global, and complex Phase I-IV clinical trials.

Culture & Benefits

  • Inclusive collaboration focused on advancing healthcare and clinical research.
  • Integrated benefits supporting physical, mental, emotional, financial, and social well-being.
  • Benefits resources designed to support employees and their families at different stages of life.

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