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11 дней назад

Data Team Lead, EMEA

Формат работы
onsite
Тип работы
fulltime
Грейд
lead
Английский
c1
Страна
UK
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
Data Team Lead, EMEA (Clinical Data Management): Managing end-to-end data management delivery for clinical research projects with an accent on data quality, project oversight, and sponsor-facing deliverables. Focus on leading study planning and execution, validating device integrations, coordinating audits and meetings, and driving technology-enabled process automation.

Location: Reading, Berkshire, United Kingdom

Company

Provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

  • Manage end-to-end data management delivery for single- and multi-service clinical projects.
  • Lead study planning, execution, close-out, milestone delivery, and financial oversight for data management activities.
  • Oversee data cleaning, validation of new device integrations, database revisions, and delivery quality.
  • Track project progress, identify risks, and coordinate corrective actions to maintain timelines and deliverables.
  • Lead internal study meetings, sponsor meetings, study kick-offs, and internal or sponsor audits.
  • Collaborate with programming and cross-functional teams on process innovation and automation.

Requirements

  • Bachelor’s degree in health, clinical, biological, mathematical sciences, or a related field.
  • 3–4 years of direct data management experience, including at least 1 year as a CDM project lead.
  • Fluent spoken English and advanced English proficiency.
  • Advanced proficiency with Microsoft Excel, Word, email, and other computer applications.
  • Advanced understanding of the drug development lifecycle and clinical research processes.
  • Ability to lead project communications, training, quality reviews, and operating procedure updates.

Culture & Benefits

  • Collaborative communication with line management and cross-functional colleagues.
  • Structured compliance with required training and electronic standard operating procedures.
  • Opportunity to contribute expert input to core operating procedures and working instructions.

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