Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Обязанности и требования для специалиста среднего уровня описаны понятно, а работа связана с клиническими исследованиями; при этом фокус роли узкий и сосредоточен на обработке выплат.
Чёткий круг задач
Медицинские исследования
Развитие и обучение
?Удалённо по Болгарии
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Clinical Payment Specialist II (Clinical Research): Managing clinical trial site grant payments and financial system setup for biotech, medtech, and specialty pharma studies with an accent on payment accuracy, forecasting, accruals, and study specifications. Focus on resolving invoice discrepancies, supporting audits and study teams, and training Clinical Payment Specialist I colleagues.
Location: Remote from Sofia, Bulgaria
Company
hirify.global supports biotech, medtech, and specialty pharma companies in developing medicines, medical devices, and diagnostics through clinical research services.
What you will do
Facilitate and distribute clinical trial grant payments to study sites and communicate with investigators, sponsors, and internal study teams.
Set up clinical studies in finance systems using study specifications, EDC visit and procedure structures, and site contracts.
Process finance-system data to produce accurate payment, forecasting, and accrual outputs within service-level timelines.
Investigate invoice discrepancies and past-due invoices, coordinate with clinical teams, and request site refunds.
Prepare payment reports, support customer audits of site payments and sponsor deposits, and provide system support throughout studies.
Improve internal implementation and investigator-grant processes and train Clinical Payment Specialist I colleagues.
Requirements
Bachelor’s degree or international equivalent from an accredited institution in finance, clinical, science, or health-related studies, or related experience.
BS/BA with 2–5 years of direct experience, or 5+ years of related experience in finance or the clinical trial industry.
Prior experience using computerized information systems.
Knowledge of clinical contracts, budget terms, and basic study start-up and management activities.
Strong analytical and investigative skills.
Strong ability to use new systems and demonstrate proficiency within them.
Nice to have
Experience with EDC, CTMS, IVRS, and other clinical systems.
Knowledge of ICH and local regulatory-authority regulations for drug research and development.
Culture & Benefits
Full-time remote work from Bulgaria.
Flexibility and work-life balance support.
Opportunities for professional growth, skill development, and career advancement.
A collaborative environment where employee ideas and feedback influence internal processes.
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