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5 дней назад

Snr Clinical Database Designer (Clinical Research)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
SA
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
Snr Clinical Database Designer (Clinical Research): Designing and configuring clinical study databases, eCRFs, edit specifications, and EDC build components with an accent on InForm, SDTM/CDASH alignment, and study delivery. Focus on coordinating design reviews, managing project risks and financials, supporting multiple platforms, and improving clinical data management processes.

Location: Bloemfontein, South Africa; other listed locations include Bellville and Centurion, South Africa. On-site role.

Company

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

What you will do

  • Interpret study protocols and design clinical databases and eCRFs using third-party or in-house CDMS tools.
  • Create and maintain edit specification documents and specifications for EDC build components, including rights, roles, system settings, and home pages.
  • Design InForm databases for LLRR data collection and ensure appropriate access for data entry and updates.
  • Participate in pre-design, screen review, data review, and internal design meetings; lead meetings where required.
  • Coordinate with data team leads, programmers, validation teams, vendors, statisticians, and client representatives.
  • Manage project risks, timelines, quality issues, financial inputs, multiple concurrent studies, and process improvement initiatives.

Requirements

  • Bachelor’s degree in science, computer science, information technology, or technology.
  • 7+ years of total experience, including 2–4 years of relevant technical designer experience.
  • Experience with clinical study database design, EDC build activities, edit specifications, and CDMS tools.
  • Ability to work across multiple study design projects and platforms.
  • Ability to identify project risks, escalate quality issues, and maintain required training and standard operating procedure compliance.

Culture & Benefits

  • Work involves collaboration with cross-functional clinical research and client-facing stakeholders.
  • Opportunity to contribute to continuous process improvement initiatives.
  • Responsibilities include structured project-specific training and adherence to standard operating procedures.

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