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2 дня назад

Clinical Research Project Manager I

76 910 - 85 295$
Формат работы
hybrid
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
Clinical Research Project Manager I (Clinical Trials/Oncology): Managing multi-center, PI-initiated clinical trials across startup, active, and close-out phases with an accent on regulatory compliance, trial documentation, and cross-functional coordination. Focus on maintaining Trial Master Files, developing protocols and consent forms, managing case report forms and databases, and tracking milestones, safety events, and project variances.

Location: Boston, Massachusetts, United States; hybrid with 2–3 days onsite per week

Salary: $76,910–$85,295 per year

Company

hirify.global conducts cancer research and provides comprehensive patient care while advancing treatments and educating physician-researchers.

What you will do

  • Manage the daily operations, budgets, resources, timelines, and milestones of assigned clinical trials.
  • Coordinate startup, active, and close-out phases for primarily PI-initiated and multi-center studies.
  • Develop and maintain Trial Master Files in accordance with Good Clinical Practice standards and institutional policies.
  • Assist Principal Investigators with protocols, consent forms, amendments, case report forms, reports, and data summaries.
  • Maintain study databases and support data integrity, regulatory submissions, safety-event tracking, and communication with regulatory authorities.
  • Coordinate research meetings, conference calls, mailings, training, and collaboration with internal and external stakeholders.

Requirements

  • Bachelor's degree relevant to clinical research.
  • Three years of experience in clinical research or project management, ideally involving multi-center oncology trials.
  • Basic understanding of clinical trial processes, regulatory requirements, and Good Clinical Practice guidelines.
  • Familiarity with clinical trial management tools such as EPIC and OnCore.
  • Strong organizational, time-management, documentation, communication, and problem-solving skills.
  • Ability to work onsite in Boston 2–3 days per week and collaborate effectively with research staff, regulatory authorities, cross-functional teams, and external partners.

Nice to have

  • Experience working in an academic institution.
  • Experience coordinating and managing clinical research operations.

Culture & Benefits

  • Inclusive, diverse, and equitable environment focused on compassionate patient care.
  • Work supporting cancer research, treatment advances, and public health programs.
  • Collaboration with Harvard Medical School-affiliated hospitals and external research partners.
  • Commitment to ethical clinical research and patient confidentiality.

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