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4 дня назад

CRA - Sponsor Aligned (Clinical Research)

74 500 - 175 100$
Формат работы
onsite
Тип работы
fulltime
Грейд
junior
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
CRA - Sponsor Aligned (Clinical Research): Monitoring and managing clinical trial sites to ensure protocol compliance, accurate study data, and adherence to GCP, ICH, and regulatory requirements with an accent on site visits, recruitment tracking, and study documentation. Focus on evaluating site quality, resolving data queries, maintaining TMF and ISF records, and coordinating study execution with clinical research teams.

Location: Overland Park, Kansas, United States

Salary: $74,500–$175,100 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

  • Perform site selection, initiation, monitoring, and close-out visits in line with the study protocol, GCP, ICH guidelines, and regulatory requirements.
  • Manage site recruitment plans, enrollment progress, regulatory submissions, approvals, CRF completion, and data query resolution.
  • Deliver protocol and study training while maintaining regular communication with assigned sites.
  • Evaluate site quality and protocol compliance, escalating issues and creating action plans where required.
  • Maintain study documentation, visit reports, follow-up letters, TMF records, and ISF files.
  • Collaborate with study teams and support site financial management and invoice retrieval when applicable.

Requirements

  • Bachelor’s degree in a scientific or healthcare discipline, or an equivalent combination of education, training, and experience.
  • At least 1 year of on-site monitoring experience.
  • Knowledge of clinical research regulations, GCP, and ICH guidelines.
  • Good therapeutic and protocol knowledge, organizational ability, and problem-solving skills.
  • Proficiency with Microsoft Word, Excel, PowerPoint, and relevant laptop, iPhone, and iPad tools.
  • Good command of English and effective communication skills are required.

Culture & Benefits

  • Full-time employment with potential incentive plans, bonuses, and other compensation depending on the position.
  • Health and welfare benefits may be provided.
  • Work includes collaboration with clinical research sites, clients, and study teams.
  • Responsibilities may involve regular travel for on-site monitoring visits.

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