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3 дня назад

Imaging Operations Coordinator I

Формат работы
remote (только USA)
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
Imaging Operations Coordinator I (Clinical Trial Imaging): Processing, validating, tracking, and managing imaging data for clinical trials with an accent on data accuracy, protocol compliance, and study database maintenance. Focus on investigating discrepancies, coordinating with clinical sites and study teams, preparing imaging data, and supporting operational quality processes.

Location: Remote in Pennsylvania, United States

Company

hirify.global, part of Thermo Fisher Scientific, provides clinical trial imaging solutions that support clinical research and the development of life-changing therapies.

What you will do

  • Process, upload, track, review, and validate imaging and study-related data for assigned clinical trials.
  • Verify transmittal documentation, media, patient data, and web-submitted study records for completeness and protocol compliance.
  • Prepare images and maintain study databases, documentation, materials, and operational records.
  • Identify, investigate, and escalate data discrepancies while communicating with clinical sites and internal study teams.
  • Generate site communications, support troubleshooting and departmental initiatives, and contribute to process improvement.
  • Follow organizational SOPs and quality standards and complete company-sponsored training.

Requirements

  • High school diploma required; an Associate’s or Bachelor’s degree in Bioscience, Computer Science, Information Technology, or a related field is preferred.
  • At least one year of experience working with computer hardware and software applications.
  • Familiarity with PC systems, email, word processing, spreadsheets, databases, network environments, file structures, and file transfers.
  • Strong attention to detail, communication, organization, documentation, prioritization, and collaboration skills.
  • Ability to work independently, adapt to changing priorities, perform computer-based work for extended periods, and occasionally lift up to 50 lbs.
  • Ability to travel up to 5% as business needs require.

Nice to have

  • Knowledge of clinical research, drug development, clinical trial processes, or pharmaceutical industry operations.
  • Associate’s or Bachelor’s degree in a relevant field.

Culture & Benefits

  • Collaborative, fast-paced work environment focused on supporting clinical research programs.
  • Competitive compensation.
  • Medical, dental, and vision coverage.
  • Flexible and paid time off, employee assistance, and wellness programs.
  • Life and disability insurance.
  • Remote and hybrid work options where applicable.

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