Назад
Company hidden
14 часов назад

Centralized Monitoring Lead- Sponsor Dedicated (Clinical Research)

151 200 - 280 700PLN
Формат работы
onsite
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
Poland
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
Centralized Monitoring Lead- Sponsor Dedicated (Clinical Research): Leading centralized monitoring for clinical trials across protocols, sites, and therapeutic areas with an accent on study start-up, resource coordination, risk assessment, and data trending. Focus on managing monitoring alerts, resolving action items, supporting site quality, and mentoring Central Monitor and Clinical Analyst Support teams.

Location: Warsaw, Poland

Salary: PLN 151,200–280,700 annualized

Company

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

What you will do

  • Partner with Clinical Leads and local Site Monitors to execute clinical studies across protocols, sites, and therapeutic areas.
  • Coordinate study start-up and initiation activities, including site activation, training compliance, system access, and monitor resourcing.
  • Lead Central Monitors and Clinical Analyst Support staff, providing training and mentoring when required.
  • Perform ongoing risk assessment through data trending and analytics, identify quality issues, and propose mitigating actions.
  • Manage DTE alerts, study-specific triggers, action items, resources, transitions, service requests, and investigator payments.
  • Support study closeout by reconciling action items, alerts, and study-specific triggers.

Requirements

  • Bachelor’s degree in life sciences or a related field, plus at least two years of relevant clinical research experience, or an equivalent combination of education, training, and experience.
  • Advanced knowledge of clinical trial conduct and applicable clinical research regulations, including ICH GCP and relevant local laws and guidelines.
  • Familiarity with clinical operations systems and software, including Microsoft Word, Excel, and PowerPoint.
  • Strong leadership, communication, problem-solving, planning, prioritization, and attention-to-detail skills.
  • Good command of English and the ability to work effectively across cultures and geographies.
  • Ability to manage conflicting priorities and maintain effective working relationships with colleagues, managers, and clients.

Culture & Benefits

  • Full-time employment.
  • Health and welfare benefits may be provided depending on the position.
  • Incentive plans, bonuses, or other compensation may be available depending on the position.
  • Work involves collaboration across cultures and geographies.

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 →