Назад
Company hidden
4 часа назад

Clinical Study Manager (Oncology)

53 200 - 79 800
Формат работы
remote (только Italy)
Тип работы
fulltime
Грейд
senior
Английский
c1
Страна
Italy
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 Study Manager (Oncology) (Clinical Research): Managing the operational and scientific oversight, set-up, execution, and delivery of local clinical trials with an accent on oncology and onco-hematology studies, regulatory compliance, and data quality. Focus on leading cross-functional clinical teams, resolving site and data issues, and ensuring inspection-ready trial execution under ICH GCP and local regulations.

Location: Home-based in Italy; candidates must be based in the listed locations. Milan and Rome are preferred.

Salary: €53,200–€79,800 annualized base pay, depending on qualifications, experience, location, and schedule.

Company

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

What you will do

  • Manage the operational and scientific oversight, set-up, execution, and delivery of assigned clinical trials at the local level.
  • Lead day-to-day monitoring activities, clinical deliverables, study commitments, and timely delivery of high-quality data.
  • Lead and coordinate cross-functional clinical teams, including local start-up, regulatory affairs, and in-house clinical staff.
  • Review site visit reports, track site issues, and support CRAs with monitoring activities and solutions.
  • Identify data and operational risks, develop mitigation plans, and maintain study-specific plans, documents, and tools.
  • Oversee regulatory updates, progress reports, renewals, and end-of-study notifications in line with the protocol, local regulations, and ICH GCP.

Requirements

  • Bachelor’s degree in a related discipline, preferably life sciences.
  • Five or more years of clinical research experience, including at least four years of project management experience or equivalent experience.
  • Previous therapeutic-area experience in Oncology or Onco-hematology is required.
  • Knowledge of ICH GCP, relevant local regulations, drug development processes, clinical operations, and inspection readiness.
  • Proven ability to lead and motivate cross-functional teams while delivering trials on time, within budget, and to the required quality.
  • Excellent spoken and written English and Italian are required. Strong decision-making, interpersonal, adaptability, and IT-system skills are also needed.

Culture & Benefits

  • Home-based work arrangement in Italy.
  • Collaboration with a sponsor-dedicated Clinical Functional Service Partnerships team and a key client.
  • Opportunity to manage clinical research projects across different therapeutic areas.
  • Health, welfare, incentive, bonus, and other benefits may be available depending on the position and employment conditions.

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 →