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4 дня назад

Senior Project Manager (Clinical Research)

147 300 - 220 900$
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 Project Manager (Clinical Research): Planning and delivering complex global clinical study projects with an accent on budget control, quality management, risk mitigation, and cross-functional coordination. Focus on leading trial execution, managing client and vendor relationships, ensuring eTMF inspection readiness, and resolving protocol and study issues.

Location: Remote, United States. Candidates must be legally authorized to work in the country of employment without employer sponsorship. Domestic and international travel, including overnight stays, may be required.

Salary: $147,300–$220,900 USD annually, plus eligibility for a discretionary annual bonus.

Company

hirify.global provides services for pharmaceutical, medical device, and clinical research programs.

What you will do

  • Plan, direct, coordinate, and deliver complex global clinical study projects within agreed quality, scope, budget, and timelines.
  • Act as the primary client contact and escalation point while coordinating internal functions and external vendors.
  • Manage study budgets, profitability, billing, forecasting, scope changes, and project performance metrics.
  • Develop project plans, timelines, risk mitigation strategies, status reports, and client presentations.
  • Lead quality management activities, including eTMF inspection readiness, quality notifications, and corrective and preventive action plans.
  • Lead internal and client meetings, support study-specific training, and provide ongoing feedback to functional team members.

Requirements

  • Bachelor’s degree or equivalent education and experience in a science or health-related field; an advanced degree is preferred.
  • At least 7 years of clinical research experience and 4 years of direct project management experience, or proven competencies for the position.
  • Experience managing complex and global clinical trials in pharmaceutical and/or medical device research.
  • Experience with Microsoft Office, Microsoft Project, eTMF, EDC, CTMS, and project management software.
  • Knowledge of ICH-GCP and relevant standard operating procedures, with strong planning, risk management, change management, communication, negotiation, and presentation skills.
  • Must be legally authorized to work in the United States without employer sponsorship.

Nice to have

  • Advanced degree in a science or health-related field.
  • Experience in oncology and cell and/or gene therapy.

Culture & Benefits

  • Health insurance, retirement savings benefits, life insurance, and disability benefits.
  • Parental leave and paid sick leave and vacation.
  • Annual bonus eligibility based on company discretion.
  • Work includes collaboration with clients, investigative staff, functional teams, and senior management.

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