Назад
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4 часа назад

Senior Clinical Trial Manager

161 800 - 199 800$
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
senior
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
Senior Clinical Trial Manager (Clinical Research): Managing clinical trials from study start-up through close-out with an accent on vendor oversight, clinical site management, study documentation, and regulatory compliance. Focus on identifying and mitigating study risks, controlling timelines and budgets, and leading cross-functional teams and direct reports.

Location: United States — Remote. Full-time work from home with occasional travel to hirify.global offices or other locations; approximately 10% travel may be required.

Annual salary: $161,800–$199,800 USD, plus eligibility for annual bonus and equity incentives.

Company

hirify.global is a biopharmaceutical company developing innovative treatments for rare diseases and advancing patient-focused clinical care.

What you will do

  • Manage day-to-day operational aspects of assigned clinical trials or regions, including CROs, vendors, drug supply, and clinical sites.
  • Oversee high-impact vendors, contracts, invoices, purchase orders, forecasts, and delivery timelines.
  • Develop and maintain study timelines, vendor and risk management plans, informed consent forms, monitoring plans, CRFs, reference manuals, and dashboards.
  • Lead or contribute to Study Management Team meetings and represent Clinical Operations on initiatives.
  • Identify study risks and implement mitigation strategies while overseeing the Trial Master File and essential document reviews.
  • Support study budgeting and financial accrual reviews, and manage direct reports.

Requirements

  • Bachelor’s degree or equivalent is required; a scientific or healthcare discipline is preferred.
  • Typically, 8 years of direct experience in clinical research, preferably including international study start-up through close-out experience.
  • Ability to independently lead all aspects of a clinical trial and effectively lead cross-functional teams.
  • Strong planning, organizational, communication, problem-solving, and risk-management skills.
  • Ability to build and maintain positive relationships with management, peers, vendors, and clinical sites.
  • Availability to work remotely from the United States and travel approximately 10% as required.

Culture & Benefits

  • Supportive and inclusive environment focused on learning and professional growth.
  • Generous vacation time and company-observed public holidays.
  • Volunteer days and employee wellbeing benefits.
  • Fitness reimbursement and tuition sponsorship.
  • Professional development plans, long-term incentives, and employee stock purchase plans or equivalent offerings.

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