Clinical Business Operations Analyst I or II (Clinical Research)
Контакты
Формат работы
remote (только Europe)
Тип работы
fulltime
Грейд
junior/middle
Английский
b2
Страна
Poland/Romania/CR +2 еще
excelbudget managementwordbusiness analysispharmaceuticalclinical researchclinical operationsfair market value
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
По международному рынку данных пока нет
На СНГ рынке: $2.9к/мес ($2.1к - $3.3к)
76
Хорошая вакансия
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Обязанности в клинических исследованиях и требования к опыту описаны понятно, но обозначение уровня I или II оставляет неясным точный уровень позиции.
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Понятные задачиВклад в медицинуНеясный грейдОграничение по странам
Оценка от Hirify AI
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Clinical Business Operations Analyst I or II (Clinical Research): Developing investigator site budgets and fee estimates for clinical research proposals across multiple countries with an accent on fair market value regulations, protocol interpretation, and cost analysis. Focus on building accurate country-level budgets, maintaining historical bid data, and solving complex pricing and feasibility problems using clinical operations information.
Location: Remote from Bulgaria, Hungary, Romania, Czech Republic, or Poland
Company
hirify.global supports biotech, medtech, and specialty pharma companies in developing medicines, devices, and diagnostics through clinical research and business operations services.
What you will do
Prepare moderately complex investigator budgets for new-business proposals in accordance with fair market value regulations.
Collaborate with operational, proposals, business development, and other internal stakeholders to develop budgets and meet deadlines.
Interpret study synopses and draft or final protocols to develop investigator budgets and country-level site budget estimates.
Provide investigator fee estimates using available project information, historical data, and comparable studies when customer information is limited.
Maintain quality, cost-effectiveness, regulatory compliance, and agreed timelines for investigator pricing budgets.
Document pricing processes, fair market value costs, benchmark databases, and investigator budget procedures; maintain historical bid and win/loss tracking.
Requirements
Undergraduate degree or international equivalent from an accredited institution, preferably in the sciences or a related field.
Two years of clinical research site, data management, clinical operations, or start-up experience in the pharmaceutical, biotech, or medical device industry.
One year of contracts and/or grant management experience.
Strong analytical, problem-solving, and critical-thinking skills, including the ability to identify efficient solutions for complex problems and improvement opportunities.
Advanced computer skills with Microsoft Office, including Excel and Word.
Strong communication and writing skills.
Culture & Benefits
Full-time remote work from Bulgaria, Hungary, Romania, Czech Republic, or Poland.
Flexible working conditions designed to support personal balance and professional growth.
Opportunities to develop skills and contribute ideas that influence how work is performed.
Work connected to clinical innovation and the development of medicines, devices, and diagnostics.
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