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3 дня назад

Research Project Coordinator I

51 281 - 64 096$
Формат работы
onsite
Тип работы
fulltime
Грейд
junior
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
Research Project Coordinator I (Clinical Research and Project Management): Coordinating research projects, protocols, committees, communications, seminars, and scientific publications with an accent on clinical research administration, stakeholder coordination, and operational organization. Focus on building project timelines, tracking milestones and budgets, managing IRB protocol information, and supporting complex academic medical research activities.

Location: Tufts Medical Center; normal office work environment with extended sitting, typing, and telephone use

Salary: $51,281.05–$64,096.04 per year

Company

hirify.global provides a medical-center environment for academic, clinical, and translational research activities.

What you will do

  • Coordinate communication between administrative staff, fellows, faculty, and other research stakeholders.
  • Create project plans and timelines, track action items, and follow up on milestones and deadlines.
  • Organize committee meetings, seminars, special events, guest speaker itineraries, travel arrangements, and related budgets.
  • Maintain active IRB protocol lists and compile publication, grant, clinical trial, and research accomplishment information.
  • Draft newsletters, website content, marketing materials, reports, presentations, correspondence, and publication materials.
  • Support Scientific Advisory Board committees and recommend operational improvements while maintaining compliance with hospital policies.

Requirements

  • Bachelor’s degree.
  • Two years of related experience.
  • Project management experience and the ability to plan and organize events.
  • Strong interpersonal, customer service, organizational, prioritization, and multitasking skills.
  • Meticulous attention to detail and strong data management skills.
  • Ability to work with multiple studies and protocols while handling sensitive and confidential information.

Nice to have

  • Prior experience in academic or medical research.

Culture & Benefits

  • Full-time employment.
  • Work in collaboration with researchers, medical staff, administrators, and leadership.
  • Responsibilities include compliance with hospital quality assurance, safety, and infection control procedures.
  • Compensation is determined based on experience, certifications, education, skills, and internal equity.
  • Total Rewards support health, financial security, and career growth.

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