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6 дней назад

Clinical Payment Specialist II (Clinical Research)

Формат работы
remote (только Bulgaria)
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
Bulgaria
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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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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