Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
Пожаловаться
Зарплата и рынок
По международному рынку данных пока нет
На СНГ рынке: $2.2к/мес ($1.9к - $4.8к)
72
Хорошая вакансия
развернуть
Обязанности по координации проектов в клинических исследованиях описаны ясно, но годовой контракт и требование быстро приступить ограничивают стабильность и доступность вакансии.
Кликните для подробной информации
Контракт на годНужно быстро выйтиПонятные обязанностиЗначимая сфера
Оценка от Hirify AI
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Подключить Plus
Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Project Specialist (Clinical Research): Coordinating cross-functional clinical research project delivery, documentation, vendor budgets, and audit readiness with an accent on project communication, financial tracking, and regulatory compliance. Focus on maintaining study systems and contact lists, managing invoices and change orders, and supporting projects under ICH/GCP, FDA, EU, and ISO 14155 requirements.
Location: Remote in Poland
Salary: minimum annualized starting base pay of 95,000 PLN
Company
hirify.global supports biotech, medtech, and specialty pharma companies in developing medicines, medical devices, and diagnostics.
What you will do
Coordinate cross-functional project teams with the Project Manager to support overall project delivery.
Facilitate internal and external communications, schedule meetings, prepare agendas, capture minutes, and maintain action and decision logs.
Maintain project documentation, contact lists, study newsletters, project systems, SOP indices, team lists, access requests, and email distribution lists.
Ensure projects are audit ready and support vendor management activities.
Requirements
Associate’s degree or equivalent in life sciences, Medicine, Pharmacy, Nursing, or a related field plus at least 2 years of clinical research experience; or a Bachelor’s degree or international equivalent plus at least 1 year of professional experience in clinical research, healthcare, business, finance, and/or project management.
Basic knowledge of ICH/GCP regulations.
Working knowledge of FDA guidance documents, EU directives, ISO 14155 regulations, drug and device development, and clinical monitoring procedures.
Basic knowledge of project management terminology and guidelines.
Strong computer skills in the MS Office suite.
Immediate availability or a short notice period is required for consideration.
Culture & Benefits
One-year fixed-term contract on hirify.global payroll.
Remote work with flexibility and work-life balance.
Opportunities for professional growth, skills development, and career advancement.
Benefits may include health insurance, life insurance, a retirement plan, paid time off, and an Employee Assistance Program.
Ideas and employee input are encouraged.
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 →