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7 дней назад

Specimen Management Associate II

35 900 - 74 800$
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
Specimen Management Associate II (Clinical Laboratory Operations): Managing incoming and outgoing biological samples to maintain accurate identification, reconciliation, labeling, storage, and complete traceability with an accent on regulatory compliance and issue resolution. Focus on reconciling shipments, resolving routine discrepancies, communicating with customers, and supporting laboratory quality and safety procedures.

Location: Austin, Texas, United States of America; Monday–Friday, 8:00 a.m.–5:00 p.m., with biweekly Saturday overtime encouraged but not mandatory.

Salary: $35,900–$74,800 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

  • Reconcile sample shipments and resolve routine issues involving identification, sorting, labeling, testing, and storage.
  • Maintain accurate sample tracking, traceability, and accountability.
  • Identify errors and potential problems, escalating concerns to senior staff.
  • Notify customers about sample receipt and respond to routine inquiries.
  • Support after-hours alarms, supply notifications, and other job-critical laboratory functions.
  • Follow company procedures, safety and quality initiatives, 6S requirements, and applicable regulatory guidelines.

Requirements

  • Bachelor’s degree in chemistry, biology, clinical laboratory science, or medical technology, or 60 college credit hours including at least 24 semester hours in natural science or medical laboratory coursework.
  • Basic knowledge of laboratory systems and procedures, with the ability to resolve routine challenges.
  • Experience with sample shipment reconciliation, identification, sorting, labeling, testing, or storage workflows; shipping experience may be accepted.
  • Knowledge of GLP/GDP regulations and experience with data entry.
  • Proficiency in Microsoft Outlook, Word, and Excel; Watson experience is beneficial, with Excel accepted as an equivalent.
  • Strong attention to detail, organization, communication, and ability to work independently and cross-functionally.

Culture & Benefits

  • Inclusive collaboration focused on advancing healthcare research and development.
  • Employee benefits and resources supporting physical, mental, emotional, financial, and social well-being.
  • Continuing education through self-study, training sessions, and meetings.
  • Work includes variable biological sample volumes, including higher-volume batch days and operational support days.

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