Назад
Company hidden
обновлено 3 дня назад

Senior Project Services Coordinator (Clinical Research)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Argentina
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
Senior Project Services Coordinator (Clinical Research): Supporting clinical studies from start-up through close-out with an accent on study coordination, laboratory monitoring setup, site activity tracking, and stakeholder communications. Focus on resolving protocol queries, identifying performance trends, coordinating study documentation, and improving project processes.

Location: Buenos Aires, Argentina

Company

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

What you will do

  • Support study setup and planning by attending meetings, preparing minutes and action logs, and drafting protocol-specific laboratory instructions.
  • Help establish protocol-specific Laboratory Centralized Monitoring requirements under Project Manager supervision.
  • Maintain studies through site loading, Investigator Portal support, kit shipment coordination, and monitoring of day-to-day performance.
  • Coordinate with internal and external stakeholders to resolve queries, protocol questions, issues, and escalations.
  • Use status reports and monitoring outputs to identify trends in investigator site performance and service delivery.
  • Support document quality control, monitoring plans, study reports, customer communications, close-out activities, and process improvements.

Requirements

  • High School Diploma or equivalent required; a Bachelor's Degree in life sciences or a related field is preferred.
  • At least 1 year of experience coordinating studies in a clinical research environment.
  • At least 1 year of experience with project management methodologies.
  • Experience using investigator portals and study tracking or status reporting tools.
  • Proficiency with Microsoft Word, PowerPoint, and Excel.
  • Strong written and verbal English communication skills required, along with organization, time management, critical thinking, and problem-solving abilities.

Culture & Benefits

  • Inclusive collaboration focused on advancing healthcare research and development.
  • Benefits and resources supporting physical, mental, emotional, financial, and social well-being.
  • Benefits programs designed to support employees and their families.
  • Full-time employment.

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 →