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4 дня назад

Clinical Research Associate II (Eyecare/Aesthetics/Specialty)

84 500 - 162 000$
Формат работы
onsite
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
Clinical Research Associate II (Eyecare/Aesthetics/Specialty) (Clinical Research): Managing clinical trial site relationships, monitoring, training, recruitment, data quality, and regulatory compliance for eyecare, aesthetics, and specialty studies with an accent on patient safety, site engagement, and study performance. Focus on conducting risk-based monitoring, resolving site risk signals, ensuring inspection readiness, and mentoring less experienced CRAs.

Location: Miami/Fort Lauderdale, Florida, United States

Salary: $84,500–$162,000 annual base pay

Company

hirify.global develops medicines and healthcare solutions across immunology, oncology, neuroscience, and Allergan Aesthetics.

What you will do

  • Serve as the primary contact for investigative sites and build effective partnerships with investigators and site staff.
  • Conduct site evaluation, training, routine monitoring, and site closure activities in accordance with protocols, GCP, ICH guidelines, regulations, and hirify.global procedures.
  • Support patient recruitment and retention, protocol compliance, data quality, safety reporting, and timely submission of study data.
  • Develop site engagement strategies, track progress through CRM tools, and identify new investigators and qualified study sites.
  • Perform continuous risk assessment, identify site risk signals, and implement corrective and preventive actions.
  • Mentor and train less experienced clinical research associates and contribute to study initiatives.

Requirements

  • Health-related tertiary qualification in medical, scientific, or nursing disciplines preferred.
  • At least 1 year of clinically related experience, including 6 months of clinical research monitoring for investigational drug or device trials.
  • Experience with risk-based, onsite, and offsite monitoring.
  • Knowledge of regulatory and legal requirements, ICH/GCP guidelines, and clinical trial quality standards.
  • Strong planning, organizational, communication, presentation, collaboration, and critical-thinking skills.
  • Ability to work effectively in a dynamic environment with competing projects and deadlines.

Culture & Benefits

  • Work focused on advancing clinical research and developing treatments for serious health conditions.
  • Paid vacation, holidays, and sick leave.
  • Medical, dental, and vision insurance for eligible employees.
  • 401(k) and eligibility for short-term incentive programs.
  • Commitment to integrity, innovation, inclusion, and equal employment opportunity.

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