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5 дней назад

Manager, Quality Control & Data Entry (Clinical Data)

Формат работы
onsite
Тип работы
fulltime
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
Manager, Quality Control & Data Entry (Clinical Data): Managing quality control and data entry workflows for early clinical research studies with an accent on regulatory compliance, staff leadership, and client delivery timelines. Focus on reviewing source and raw data, improving data-flow processes, resolving error trends, and presenting QC processes to sponsors and auditors.

Location: Tempe, Arizona, United States; onsite

Company

hirify.global conducts early clinical research and uses translational medicine, research expertise, and innovative strategies to support faster drug development.

What you will do

  • Manage quality control and data entry workflows for clinical research studies.
  • Lead, supervise, train, coach, and evaluate QC and data entry staff.
  • Plan workloads, schedules, study timelines, and client deliverables in line with regulatory and internal requirements.
  • Perform or oversee source-data and raw-data QC reviews, accurate data entry, and study setup activities.
  • Write and review QC and data entry SOPs and procedure guides, and track operational metrics.
  • Lead process improvement and problem-solving initiatives, participate in audits and inspections, and present QC processes to sponsors.

Requirements

  • Bachelor’s degree in a related field required.
  • 1–2 years of supervisory, trainer, or team-lead experience.
  • Knowledge of Good Clinical Data Management Practices, medical terminology, GCP, ICH Guidelines, and 21 CFR Part 11 preferred.
  • Strong process improvement, change management, critical thinking, and problem-solving skills.
  • Clinical data experience preferred.
  • Ability to adjust working hours to meet workload priorities.

Culture & Benefits

  • Values include integrity, trust, teamwork, and respect.
  • Work involves collaboration with internal departments, study sites, sponsors, and auditors.
  • Equal opportunity employment environment.

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