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8 дней назад

Imaging Operations Coordinator I

Формат работы
hybrid
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/Data Management): Processing, validating, tracking, and managing imaging data for assigned clinical trials with an accent on data accuracy, protocol compliance, and study record integrity. Focus on investigating discrepancies, maintaining study databases, coordinating with clinical sites, and supporting operational quality improvements.

Location: Hybrid work from the offices in Philadelphia, United States; up to 5% travel may be required.

Company

hirify.global, part of Thermo Fisher Scientific, provides advanced clinical trial imaging solutions that support clinical research and evidence generation.

What you will do

  • Process imaging and study-related data for assigned clinical trials.
  • Review, track, monitor, and validate data received from clinical sites for accuracy, completeness, and protocol compliance.
  • Verify transmittal documentation, patient data, and study materials; enter and upload information into study databases.
  • Prepare images, process web-submitted data, maintain study records, and generate site communications.
  • Investigate and escalate data discrepancies while communicating with clinical sites and internal study teams.
  • Maintain documentation, prepare and ship study materials, support troubleshooting, and participate in process improvement initiatives.

Requirements

  • High school diploma required; an Associate’s or Bachelor’s degree in Bioscience, Computer Science, Information Technology, or a related field is preferred.
  • Availability to work on a hybrid basis from the Philadelphia offices is required.
  • 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 perform computer-based work for extended periods and occasionally lift up to 50 lbs.

Nice to have

  • Knowledge of clinical research, drug development, clinical trial processes, or pharmaceutical industry operations.

Culture & Benefits

  • 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.
  • Company-sponsored training and an inclusive, equal opportunity work environment.

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