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10 дней назад

Solutions Design Analyst (eCOA)

Формат работы
remote (только USA)
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
Solutions Design Analyst (eCOA): Delivering electronic Clinical Outcome Assessment solution designs for pharmaceutical and biotechnology clinical studies with an accent on protocol analysis, requirements translation, and data integrity. Focus on defining study-specific designs, maintaining specifications across data capture and database structures, and coordinating testing and project delivery.

Location: United States Remote

Company

hirify.global, part of Thermo Fisher Scientific, provides clinical technology and evidence solutions for pharmaceutical and biotechnology clients.

What you will do

  • Coordinate the overall solutions design process for client clinical studies.
  • Review clinical trial protocols, questionnaires, and related documentation to define study-specific eCOA designs.
  • Gather sponsor requirements and recommend design components that meet clinical study needs.
  • Create and maintain design specifications across data capture, delivery, and database structures.
  • Collaborate with Project Management, Data Management, Product, and Clinical Systems Translation & Licensing teams to align requirements and protect data integrity.
  • Present solution designs at internal and external milestone meetings and support scoping, change control, testing, documentation, and process improvement.

Requirements

  • Bachelor’s degree or equivalent; a science or healthcare-related degree is preferred.
  • At least 3 years of experience in clinical trials or an equivalent role.
  • Ability to interpret clinical trial protocols, questionnaires, and data models.
  • Experience translating client requirements into design specifications.
  • Strong collaboration, communication, problem-solving, organization, and attention-to-detail skills.
  • Familiarity with FDA regulatory processes and clinical research standards; proficiency with Microsoft Office Suite.

Nice to have

  • Experience with technical documentation tools.

Culture & Benefits

  • Competitive compensation.
  • Medical, dental, and vision insurance beginning on the first day.
  • Flexible work schedules and remote or hybrid work options.
  • Attractive paid time off package.
  • Opportunity to contribute to clinical science, technology, and initiatives that support faster delivery of therapies to patients.

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