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10 дней назад

Clinical Research Associate II (Clinical Research)

Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US/Argentina
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
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TL;DR
Clinical Research Associate II (Clinical Research): Monitoring clinical trial sites and partnering with investigators and site staff to ensure protocol compliance, data integrity, patient safety, and study performance with an accent on risk-based monitoring, regulatory requirements, and site engagement. Focus on identifying and mitigating site risks, supporting recruitment and retention, maintaining inspection readiness, and mentoring less experienced CRAs.

Location: Buenos Aires, Argentina

Company

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

What you will do

  • Serve as the primary point of contact for investigative sites and build effective partnerships with investigators and site staff.
  • Align, train, and motivate site personnel on clinical trial goals, protocols, and patient treatment principles.
  • Conduct site evaluation, training, routine monitoring, and site closure activities in accordance with protocols, monitoring plans, GCP, ICH Guidelines, SOPs, and quality standards.
  • Assess site performance and risk signals, implement corrective and preventive action plans, and support patient safety and protocol compliance.
  • Evaluate investigators and sites, support patient recruitment and retention, and ensure timely, accurate safety and clinical data submissions.
  • Mentor less experienced CRAs and contribute to global or local task forces and initiatives.

Requirements

  • Tertiary qualification in a health-related discipline such as medicine, science, or nursing is preferred.
  • At least 1 year of clinically related experience, including at least 6 months monitoring investigational drug or device trials.
  • Experience with risk-based, onsite, and offsite clinical trial monitoring.
  • Knowledge of local regulatory and legal requirements, ICH/GCP Guidelines, and applicable policies.
  • Strong planning, organizational, communication, presentation, critical thinking, and stakeholder collaboration skills.
  • Ability to work effectively with clinical site issues, competing projects, and deadlines while maintaining integrity and quality.

Culture & Benefits

  • Work focused on advancing clinical research and turning scientific discoveries into medicines.
  • Opportunity to contribute to immunology, oncology, neuroscience, and aesthetics programs.
  • Equal opportunity employment with a stated commitment to integrity, innovation, and community service.

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