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обновлено 8 дней назад

Clinical Trial Manager (Healthcare)

112 000 - 140 000$
Формат работы
remote (только USA)/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 Trial Manager (Healthcare): Leading the end-to-end execution of clinical trials for precision medicine solutions with an accent on site activation, regulatory compliance, and vendor management. Focus on driving study performance, mitigating operational risks, and ensuring high-quality data delivery across the patient journey.

Location: Remote within the United States; 10–30% travel expected.

Salary: $112,000–$140,000 USD annually for remote US roles.

Company

hirify.global develops precision medicine, genomics-based testing, and digital healthcare solutions for organ transplant patients and caregivers.

What you will do

  • Lead end-to-end clinical trial execution, from site identification and study start-up through monitoring, closeout, and clinical study reporting.
  • Manage study timelines, budgets, metrics, site activation, enrollment, submissions, documentation, and study-specific meetings.
  • Identify operational, quality, and timeline risks; lead mitigation plans, escalations, and resolution activities.
  • Coordinate Clinical Operations, Data Management, Medical Affairs, clinical sites, CROs, central laboratories, and external vendors.
  • Oversee eTMF and CTMS usage, data quality, inspection readiness, study tracking, and performance reporting.
  • Directly manage, coach, and develop clinical operations personnel while improving study execution processes and SOPs.

Requirements

  • Bachelor’s degree in life sciences, health sciences, or equivalent education and experience.
  • At least 4 years of clinical trial management experience and 2+ years of clinical research associate experience with on-site or remote monitoring.
  • At least 2 years of direct management, coaching, and development of clinical operations professionals.
  • Strong knowledge of ICH/GCP and FDA regulatory requirements, medical terminology, clinical documentation, and laboratory testing.
  • Strong clinical study, project management, communication, leadership, problem-solving, and organizational skills.
  • Proficiency with Microsoft Office, EDC platforms such as Medrio or Medidata, eTMF, CTMS, and safety reporting systems.

Nice to have

  • RN or pharmaceutical experience.
  • Experience with clinical studies involving organ transplantation.

Culture & Benefits

  • Remote work for US-based employees with expected travel of 10–30%.
  • Health and welfare benefits, including gym reimbursement.
  • 401(k) matching, employee stock purchase plan, and pre-tax commuter benefits.
  • Competitive base salary and incentive compensation.
  • Up to 30 days of paid annual leave for eligible full-time employees who donate an organ or bone marrow.

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