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2 дня назад

Clinical Research Project Manager - Breast Oncology

76 910 - 85 295$
Формат работы
hybrid
Тип работы
fulltime
Грейд
middle
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 - Breast Oncology (Clinical Trials): Managing multi-center, PI-initiated breast oncology 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, designing case report forms, and tracking project milestones, safety events, and study databases.

Location: Fully remote from a New England state (ME, VT, NH, MA, CT, or RI) with occasional onsite time in Boston, Massachusetts.

Salary: $76,910–$85,295 per year.

Company

hirify.global conducts cancer research, provides patient care, and develops treatments through partnerships with Harvard Medical School-affiliated hospitals.

What you will do

  • Manage day-to-day operations, budgets, resources, timelines, and milestones for assigned breast oncology clinical trials.
  • Coordinate startup, active, and close-out phases of multi-center and PI-initiated trials.
  • Develop and maintain Trial Master Files and other essential regulatory documentation in line with GCP standards.
  • Assist the Principal Investigator with protocols, consent forms, amendments, reports, and data summaries.
  • Design case report forms and maintain study databases with accurate, compliant data.
  • Train research staff, coordinate meetings, track safety events, and communicate with stakeholders and regulatory authorities.

Requirements

  • Bachelor's degree in a field relevant to clinical research.
  • At least 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 organization, communication, documentation, problem-solving, and time-management skills.
  • Ability to work remotely only from Maine, Vermont, New Hampshire, Massachusetts, Connecticut, or Rhode Island, with occasional onsite attendance in Boston.

Nice to have

  • Experience working in an academic institution.
  • Experience coordinating and managing oncology clinical trials.

Culture & Benefits

  • Full-time position with a primarily remote work arrangement.
  • Work within an innovative, inclusive, and equitable cancer research and patient-care environment.
  • Collaborate with faculty, research staff, external partners, and Harvard Medical School-affiliated hospitals.

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