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9 дней назад

Clinical Research Manager - Breast Oncology Clinical Trials

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 - Breast Oncology Clinical Trials (Clinical Research): Managing therapeutic and non-therapeutic breast oncology clinical trials with an accent on regulatory compliance, data quality, patient safety, and staff supervision. Focus on overseeing trial portfolios, resolving operational and regulatory challenges, monitoring clinical research data, and managing study finances and personnel.

Location: Hybrid, with two or three days onsite per week in Boston, Massachusetts; remote days may only be worked from Maine, Vermont, New Hampshire, Massachusetts, Connecticut, or Rhode Island.

Salary: $77,400–$102,800 per year

Company

hirify.global conducts cancer research, provides patient care, and advances treatment through education and collaboration with Harvard Medical School-affiliated hospitals.

What you will do

  • Manage the Breast Oncology clinical research portfolio and oversee therapeutic and non-therapeutic clinical trials under Good Clinical Practice.
  • Design, implement, and evaluate clinical research activities in collaboration with physicians, research nurses, the Clinical Trials Office, and other institutional groups.
  • Oversee protocol submissions, essential documents, safety reporting, annual approvals, deviations, and other regulatory and compliance requirements.
  • Track enrollment, treatment, follow-up care, clinical trial performance benchmarks, data quality, and clinical trial management system activity.
  • Support protocol budgets, grant reporting, financial reconciliation, equipment management, and preparation of research manuscripts.
  • Recruit, supervise, train, onboard, and evaluate clinical research coordinators, students, volunteers, and research assistants.

Requirements

  • Bachelor’s degree required; at least 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, protocol development, and data compilation and analysis.
  • Knowledge of federal and state research regulations, clinical trial startup, active and closeout phases, and local clinical research policies.
  • Strong interpersonal, organizational, and communication skills, with the ability to manage personnel issues and provide critical feedback.
  • Working knowledge of Microsoft Office, Livelink, EPIC, and OnCore.

Culture & Benefits

  • Hybrid work arrangement with regular onsite collaboration in Boston.
  • Inclusive, diverse, equitable, and patient-focused work environment.
  • Opportunity to contribute to cancer research, patient care, and public health programs.
  • Equal opportunity employment.

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