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2 дня назад

Project Manager - Clinical Trial Operations Exp. Req. (Job 1421)

90 000 - 110 000$
Формат работы
remote (только USA)
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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Мэтч & Сопровод

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Описание вакансии

Текст:
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TL;DR
Project Manager - Clinical Trial Operations Exp. Req. (Job 1421) (Clinical Research): Managing end-to-end clinical trial operations for the ACTG Clinical Trials Network with an accent on study start-up, site coordination, protocol implementation, enrollment tracking, and study close-out. Focus on coordinating multi-site research programs, ensuring regulatory compliance, and solving complex operational and project delivery issues.

Location: United States - Remote

Salary: $90,000–$110,000 yearly, plus potential performance incentives and program-specific awards.

Company

hirify.global delivers health, national security readiness, scientific research, systems engineering, and digital transformation solutions for federal programs.

What you will do

  • Provide primary project management oversight for clinical research studies within the ACTG Clinical Trials Network.
  • Manage projects from concept through implementation, including scope, objectives, work plans, schedules, estimates, resources, and status reporting.
  • Oversee study start-up, site coordination, protocol implementation, enrollment tracking, and clinical trial close-out.
  • Direct project resources, coordinate vendors, and review technical deliverables.
  • Lead project meetings, tracking, analysis, issue remediation, and quality reviews.
  • Collaborate with end users, client services, computer services, and other affected areas.

Requirements

  • Bachelor’s degree in public health, life sciences, health administration, or a related field with 4+ years of clinical trial operations experience, or a master’s degree with 2+ years of experience.
  • Strong knowledge of regulatory requirements, including GCP, ICH, and FDA/NIH guidelines.
  • Proven ability to manage complex projects collaboratively.
  • Excellent communication, organizational, analytical, and problem-solving skills.

Nice to have

  • PMP certification.
  • Experience with infectious disease clinical trials or related therapeutic areas.
  • Experience supporting large, multi-site clinical research programs or networks.

Culture & Benefits

  • Remote work within the United States.
  • Medical, dental, vision, life, disability, and flexible spending account benefits.
  • Paid time off, parental leave, and legal services.
  • 401(k) retirement plan with matching contributions.
  • Training, e-learning, certification preparation, and education assistance.

Hiring process

  • Fair and authentic interview process.
  • Reasonable accommodation is available for applicants with disabilities and disabled Veterans.

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