Назад
Company hidden
7 дней назад

Clinical Research Associate, Sponsor Dedicated

74 500 - 197 500$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US
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 Research Associate, Sponsor Dedicated (Clinical Research/GCP): Performing site monitoring and management for clinical studies, ensuring protocol compliance, data quality, recruitment progress, and regulatory documentation with an accent on Good Clinical Practice, site oversight, and clinical trial systems. Focus on conducting monitoring visits, resolving data queries, maintaining trial documentation, and coordinating study execution with sites and project teams.

Location: Durham, North Carolina, United States of America. Candidates must reside in the same country where the job is located.

Salary: $74,500–$197,500 annualized base pay, depending on qualifications, location, and schedule.

Company

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

What you will do

  • Conduct site selection, initiation, monitoring, and close-out visits in accordance with the study protocol, Good Clinical Practice, and contracted scope.
  • Support site recruitment plans, track enrollment, and manage ongoing communication with clinical research sites.
  • Deliver protocol and study training and evaluate site compliance, data quality, and integrity.
  • Track regulatory submissions, approvals, case report forms, data queries, and study progress.
  • Maintain Trial Master File and Investigator Site File documentation and prepare monitoring reports, follow-up letters, and action plans.
  • Collaborate with study teams and, where applicable, support site financial management and invoice collection.

Requirements

  • Bachelor’s degree in a scientific or healthcare discipline preferred; equivalent education, training, and experience may be accepted.
  • At least two years of independent on-site monitoring experience as a Clinical Research Associate in a CRO, sponsor, or similar environment.
  • Knowledge of clinical research regulations, Good Clinical Practice, and International Conference on Harmonization guidelines.
  • Experience using EDC, CTMS, eTMF, IVRS/IWRS, and other clinical trial systems.
  • Good command of English, with strong written and verbal communication skills.
  • Strong organizational, problem-solving, time-management, financial-management, and relationship-building skills.

Culture & Benefits

  • Full-time employment with health, welfare, and other benefits.
  • Potential incentive plans, bonuses, and additional compensation may be available depending on the position.
  • Work supports the development and commercialization of medical treatments and improved patient outcomes.

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