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9 дней назад

Associate Clinical Trials Specimen Management Technician

16 - 18$
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
Associate Clinical Trials Specimen Management Technician (Clinical Trials Specimen Management): Processing, sorting, storing, and shipping clinical trial specimens in an onsite laboratory with an accent on temperature-controlled handling, shipment documentation, and regulatory compliance. Focus on managing samples at ultra-cold and liquid-nitrogen temperatures, maintaining specimen records, and preparing shipments for reference laboratories.

Location: Onsite in Rochester, NY; Tuesday–Saturday day schedule, 40 hours per week

Salary: $16.00–$18.00 per hour

Company

hirify.global provides clinical trials specimen management and laboratory processing services.

What you will do

  • Process, distribute, sort, receive, and store clinical trial specimens.
  • Open shipments, document receipt information, and prepare specimens for reference laboratories.
  • Handle samples under varying temperature conditions, including ultra-cold storage at -80°C and liquid nitrogen at -196°C.
  • Maintain freezer storage areas, clear ice buildup, empty waste ice receptacles, and keep the workspace clean.
  • Perform and document specimen rotation, temperature monitoring, pending-list checks, and other daily maintenance activities.
  • Follow applicable FDA, New York State Department of Health, Good Clinical Practice, IATA, and U.S. and foreign shipping requirements.

Requirements

  • General proficiency with email and basic computer programs.
  • Strong data entry skills.
  • Ability to stand for 3–4 hours while working.
  • Ability to lift packages weighing up to 50 pounds.
  • Ability to work safely around frozen storage equipment, liquid nitrogen, bodily fluids, and operational areas.

Nice to have

  • Associate or bachelor’s degree in biomedical sciences or a related field.

Culture & Benefits

  • Full-time schedule of 40 hours per week.
  • Day shift from Tuesday through Saturday.
  • Work in a regulated clinical trials specimen processing environment.
  • Physical capability screening may be required, with accommodations considered for reported physical limitations.

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