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2 часа назад

Clinical Research Associate (CRA 2), Sponsor Dedicated

71 900 - 182 000$
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 (CRA 2), Sponsor Dedicated (Clinical Research): Performing site monitoring and site management for clinical studies with an accent on GCP/ICH compliance, protocol adherence, and study data quality. Focus on managing recruitment, regulatory submissions, CRF completion, data queries, trial documentation, and communication with clinical sites.

Location: United States; candidates can be located anywhere in the US. The role includes onsite monitoring visits to clinical research sites.

Salary: $71,900–$182,000 annualized base pay.

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 line with study requirements and regulatory standards.
  • Manage site recruitment plans, enrollment progress, regulatory submissions, CRF completion, and data query resolution.
  • Train assigned sites on study protocols and maintain regular communication to address project expectations and issues.
  • Evaluate site practices, protocol adherence, data quality, and regulatory compliance, escalating quality issues when necessary.
  • Maintain monitoring reports, follow-up letters, site documentation, the Trial Master File, and Investigator's Site Files.
  • Collaborate with study teams and support site financial management and invoice retrieval when applicable.

Requirements

  • 1–2 years of onsite clinical research monitoring experience.
  • Bachelor's degree in a scientific discipline or healthcare preferred; equivalent education, training, and experience may be accepted.
  • Knowledge of clinical research regulations, Good Clinical Practice (GCP), and International Council for Harmonisation (ICH) guidelines.
  • Therapeutic and protocol knowledge in areas such as cardiovascular, renal, metabolic, oncology, and/or neurology.
  • Good written and verbal English communication skills, organizational and problem-solving abilities, and effective time and financial management.
  • Proficiency with Microsoft Word, Excel, PowerPoint, and relevant laptop, iPhone, and iPad use.

Culture & Benefits

  • Full-time employment with potential health, welfare, and other benefits.
  • Additional incentive plans, bonuses, or other compensation may be available depending on the position.
  • Work supports clinical research and the development of innovative medical treatments.

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