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5 дней назад

Senior Clinical Research Associate (Clinical Research)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US/Taiwan
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
Senior Clinical Research Associate (Clinical Research): Ensuring protocol-level execution of clinical studies across site start-up, monitoring, execution, and close-out with an accent on regulatory compliance, audit readiness, and site performance. Focus on identifying site risks, maintaining clinical trial systems, mentoring CRAs, and supporting complex global and local study initiatives.

Location: Taipei, Taiwan

Company

hirify.global develops innovative medicines and solutions across immunology, oncology, neuroscience, and aesthetics.

What you will do

  • Execute assigned clinical studies from site start-up through monitoring, close-out, and reporting.
  • Conduct site evaluations, selection, activation, monitoring visits, and follow-up while identifying risks and developing mitigation plans.
  • Maintain clinical trial management systems and manage site payments according to study agreements and local requirements.
  • Ensure compliance with regulations, Good Clinical Practice, ICH Guidelines, monitoring plans, and standard operating procedures.
  • Prepare sites for audits and inspections, support CAPA activities, and maintain inspection readiness.
  • Coach and mentor CRAs and contribute to study task forces, training initiatives, and remote data review when assigned.

Requirements

  • Bachelor’s degree or equivalent in a health-related field such as medicine, science, nursing, or pharmacy.
  • At least 5 years of site monitoring experience.
  • Strong analytical, critical-thinking, planning, organizational, interpersonal, and communication skills.
  • Flexibility, adaptability, resourcefulness, creativity, and the ability to manage competing projects and deadlines.
  • Demonstrated teamwork, business ethics, and integrity.

Culture & Benefits

  • Work within a global research and development organization focused on innovative medicines.
  • Opportunity to contribute to clinical studies across local and global initiatives.
  • Responsibilities may include CRA mentoring, training development, and collaboration with CROs and study stakeholders.
  • Equal opportunity employment environment committed to integrity, innovation, and community impact.

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