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9 часов назад

Clinical Project Manager (Clinical Research)

Формат работы
remote (только USA)
Тип работы
fulltime
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 Project Manager (Clinical Research): Leading cross-functional clinical research projects from study start-up through closeout with an accent on operational execution, stakeholder coordination, financial tracking, and regulatory compliance. Focus on managing clinical trial timelines, risks, resources, project teams, and study requirements across sponsors, sites, and internal stakeholders.

Location: United States Remote; remote and hybrid work options are available.

Company

hirify.global, part of Thermo Fisher Scientific, provides endpoint data solutions that support clinical research and accelerate the development of life-changing therapies.

What you will do

  • Lead clinical study start-up activities, including protocol review, project planning, timelines, milestones, and documentation.
  • Manage project communications, stakeholder updates, reporting schedules, risks, resources, and operational challenges.
  • Oversee project finances, including forecasting, billing, scope reviews, amendments, revenue reporting, and pass-through costs.
  • Coordinate data collection across sites and ensure compliance with protocols, SOPs, regulations, and quality requirements.
  • Lead and support project teams through expectation-setting, training, mentoring, and collaboration.
  • Oversee study closeout, support business development activities, and drive continuous improvement initiatives.

Requirements

  • Bachelor’s degree in Life Sciences, Pharmacy, Nursing, Healthcare, or a related field, or an equivalent combination of education and experience.
  • Experience managing clinical research projects involving investigational products in a CRO or pharmaceutical environment.
  • Clinical trial experience with the ability to manage multiple projects, timelines, and stakeholders.
  • Working knowledge of GCP, ICH guidelines, and FDA regulations.
  • Experience with project planning, budgeting, forecasting, financial tracking, and resource management.
  • Proficiency with Microsoft Word, Excel, and Project, plus strong communication, presentation, leadership, organizational, and problem-solving skills.

Nice to have

  • Knowledge of medical imaging technologies or imaging-focused clinical studies.

Culture & Benefits

  • Collaborative, fast-paced, and results-driven work environment.
  • Medical, dental, and vision coverage.
  • Flexible and paid time off.
  • Tuition reimbursement and employee assistance and wellness programs.
  • Life and disability insurance.

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