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3 дня назад

Assistant Clinical Research Manager - Center of Early Detection & Intervention Blood Cancers Interventional Clinical Trials (Clinical Research)

70 000 - 85 300$
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
Assistant Clinical Research Manager (Clinical Trials): Supporting the management and oversight of interventional cancer clinical trials, including study start-up, active operations, closeout, regulatory compliance, data management, and staff supervision with an accent on Good Clinical Practice and audit-ready trial execution. Focus on tracking protocol milestones, maintaining essential documents, monitoring enrollment and data compliance, and coordinating corrective actions across clinical research stakeholders.

Location: Hybrid in Boston, Massachusetts, with 2–3 onsite days per week; remote workdays are limited to Maine, Vermont, New Hampshire, Massachusetts, Connecticut, or Rhode Island.

Salary: $70,000–$85,300 per year

Company

hirify.global conducts cancer research, clinical trials, patient care, and medical education in partnership with Harvard Medical School-affiliated hospitals.

What you will do

  • Support oversight of the Blood Cancers interventional clinical trial portfolio and related regulatory and compliance activities.
  • Coordinate study start-up, active trial operations, and closeout activities, including protocol development and milestone tracking.
  • Support patient enrollment, protocol treatment, follow-up care, registration, and interaction with study registrars and pharmaceutical sponsors.
  • Maintain essential regulatory documents and clinical trial reporting, including safety events, annual approvals, and deviations.
  • Monitor data collection, compliance status, progress reports, and corrective actions with investigators, sponsors, and clinical trial operations stakeholders.
  • Support recruitment, onboarding, training, competency assessments, and day-to-day supervision of clinical research staff.

Requirements

  • Bachelor’s degree required.
  • 3+ years of related experience preferred.
  • Understanding of clinical research, cancer treatment modalities, clinical trial start-up, active, and closeout phases.
  • Knowledge of local policy and federal and state research regulations, with the ability to identify issues requiring regulatory consultation.
  • Experience with protocol development, data compilation and analysis, tracking systems, and Microsoft Office.
  • Ability to work independently, think critically, exercise professional judgment, and communicate effectively.

Culture & Benefits

  • Inclusive, diverse, and equitable environment focused on compassionate patient care.
  • Work on research advancing cancer treatment and public health.
  • Patient contact may include individuals of all ages and populations.
  • Hybrid work arrangement with regular onsite collaboration in Boston.

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