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2 часа назад

Set Up Specialist I (Clinical Research)

Формат работы
hybrid
Тип работы
fulltime
Грейд
junior
Английский
c1
Страна
Mexico
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
Set Up Specialist I (Clinical Research): Setting up laboratory requirements for clinical trials and coordinating study specifications, timelines, databases, manuals, requisitions, and site materials with an accent on protocol compliance, client communication, and operational accuracy. Focus on interpreting complex study protocols, identifying study risks, configuring laboratory systems, and establishing best practices for new laboratory setup requirements.

Location: Hybrid, Mexico City only

Company

hirify.global is a global healthcare intelligence and clinical research organisation focused on bringing new medicines and treatments to patients faster.

What you will do

  • Act as the primary client liaison during laboratory setup for clinical trials.
  • Complete and maintain accurate Laboratory Specifications Documents based on study protocols, client requirements, ICL standards, and operational input.
  • Coordinate setup timelines, communicate major decisions and changes, and collaborate with project managers, laboratory teams, and clinical CRO stakeholders.
  • Guide clients through setup, provide solutions, identify study risks, and participate in risk assessment and operational meetings.
  • Oversee database configuration, client approval of laboratory manuals and requisitions, and preparation of visit-specific site kits and source materials.
  • Develop best practices and solutions for new and complex laboratory protocol requirements.

Requirements

  • Bachelor’s degree in life sciences, clinical research, healthcare management, or a related field.
  • At least 1 year of experience in a clinical trial environment, such as project management, site coordination, or database configuration.
  • Experience interpreting study protocols, regulatory requirements, and GCP guidelines.
  • Strong understanding of clinical trial processes and laboratory testing.
  • Excellent organisation, attention to detail, communication, and stakeholder collaboration skills.
  • Advanced English skills and proficiency in Microsoft Word, Excel, and PowerPoint.

Culture & Benefits

  • Inclusive culture based on integrity, collaboration, agility, and belonging.
  • Competitive salary and country-specific benefits.
  • Annual leave, health insurance options, retirement planning, and life assurance.
  • Global Employee Assistance Programme with 24-hour access to wellbeing professionals.
  • Optional benefits may include childcare vouchers, gym memberships, travel subsidies, and health assessments.

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