Назад
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5 дней назад

In-House Clinical Research Associate

100 000 - 120 000$
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
In-House Clinical Research Associate (Clinical Trials): Supporting clinical trial sites through start-up, recruitment, retention, execution, quality oversight, and closeout with an accent on site engagement, regulatory compliance, and clinical trial systems. Focus on activating sites, resolving EDC data queries, supporting audits and inspections, and coordinating stakeholders across clinical development and operations.

Location: Plainsboro, New Jersey, United States; 0–10% overnight travel required, with occasional work on company holidays and weekends.

Salary: $100,000–$120,000 per year, plus eligibility for a company performance bonus.

Company

hirify.global is a global healthcare and pharmaceutical company developing medicines for diabetes, obesity, rare blood and endocrine disorders, and other serious chronic diseases.

What you will do

  • Serve as the primary point of contact for clinical trial sites, providing guidance, training, and support.
  • Drive site selection, activation, regulatory document collection, staff training, and system access.
  • Track patient recruitment and support retention, EDC data entry, and data query resolution.
  • Support trial closure, data cleaning, database lock, and site closeout activities.
  • Support audits, health authority inspections, action-item follow-up, and protocol deviation reviews.
  • Contribute to Trial Core Teams, improvement projects, and collaboration with internal and external stakeholders.

Requirements

  • Bachelor’s degree in a science-related discipline or a Registered Nurse degree.
  • At least 3 years of experience planning and conducting GCP clinical trials.
  • At least 2 years of direct site management and clinical trial logistics experience.
  • Understanding of medical terminology, ICH-GCP principles, and their application to clinical trials.
  • Computer skills with MS Office and clinical trial systems, plus adaptability to new technologies.
  • Excellent written, verbal, and presentation communication skills in English, with collaborative and stakeholder management abilities.

Nice to have

  • Site activation and site management or monitoring experience.
  • Relevant hirify.global experience.

Culture & Benefits

  • Patient-centered work focused on improving long-term health outcomes.
  • Medical, dental, and vision coverage, life and disability insurance, and a 401(k) savings plan.
  • Flexible spending accounts, employee assistance, tuition reimbursement, and voluntary insurance benefits.
  • Sick time, flexible vacation, and parental leave policies.
  • Inclusive recruitment and equal employment opportunity.

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