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2 дня назад

Clinical Research Manager - Pediatric Heme Malignancy

77 400 - 102 800$
Формат работы
hybrid
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
Clinical Research Manager - Pediatric Heme Malignancy (Clinical Trials): Managing pediatric hematologic malignancy clinical trials with an accent on Good Clinical Practice, regulatory compliance, patient safety, and research staff supervision. Focus on coordinating trial operations, maintaining data quality and regulatory documentation, resolving complex study challenges, and overseeing budgets and clinical research personnel.

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

Salary: $77,400–$102,800 per year

Company

hirify.global is a cancer research and patient-care organization conducting clinical research, education, and treatment programs in partnership with Harvard Medical School-affiliated hospitals.

What you will do

  • Manage the pediatric hematologic malignancy clinical trial portfolio across therapeutic and non-therapeutic studies.
  • Coordinate protocol submissions, trial startup, active study operations, closeout activities, and regulatory reporting.
  • Oversee patient enrollment, protocol treatment, follow-up care, registration, and clinical trial management system updates.
  • Monitor data quality, compliance metrics, corrective actions, progress reports, and essential regulatory documentation.
  • Support protocol budgets, grant finances, equipment management, manuscripts, study forms, and monitoring procedures.
  • Recruit, supervise, train, onboard, and evaluate clinical research coordinators and other research staff.

Requirements

  • Bachelor’s degree and a minimum of 5 years of related experience preferred.
  • Previous supervisory experience and the ability to work independently with minimal supervision.
  • Knowledge of cancer, cancer treatment modalities, clinical trial processes, and Good Clinical Practice.
  • Experience with protocol development, data compilation and analysis, clinical trial compliance, and research tracking systems.
  • Knowledge of federal and state research regulations, regulatory documentation, and clinical trial reporting.
  • Computer skills including Microsoft Office and working knowledge of Livelink, EPIC, and OnCore.

Culture & Benefits

  • Collaborative work with physicians, clinical research managers, research nursing staff, investigators, sponsors, and clinical trials offices.
  • Work in an innovative, caring, inclusive, and equitable patient-care and research environment.
  • Exposure to groundbreaking cancer research and programs serving diverse and underserved populations.
  • Normal office working conditions with regular onsite collaboration.

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