5 дней назад
Clinical Research Coordinator - Breast Oncology Clinical Trials
48 100 - 54 400$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Clinical Research Coordinator - Breast Oncology Clinical Trials (Clinical Research/Oncology): Coordinating breast oncology clinical trials across start-up, active conduct, data management, monitoring, and close-out with an accent on protocol compliance, patient information, regulatory submissions, and trial sample handling. Focus on managing clinical data and source documents, preparing for audits, coordinating cross-functional study activities, and supporting participant interactions.
Location: Boston, Massachusetts, United States; onsite with occasional remote work
Salary: $48,100–$54,400 per year
Company
conducts cancer research, provides patient care, and advances treatment through education and collaboration with Harvard Medical School-affiliated hospitals.
What you will do
- Coordinate breast oncology clinical trials throughout the study life cycle, from protocol start-up and site activation through close-out.
- Collect, manage, enter, and report patient clinical data, source documents, case report forms, adverse events, and study activity in clinical trial management systems.
- Prepare and maintain participant and regulatory binders, IRB submissions, study records, and audit and monitoring materials.
- Collect, prepare, and ship protocol-required tissue and other samples in accordance with IATA/DOT regulations.
- Coordinate with scheduling, materials management, laboratories, pharmacy, research nursing, sponsors, regulatory authorities, and other departments.
- Screen participants, support informed consent for non-treatment trials, register study participants in ONCORE, and conduct protocol-directed patient interactions.
Requirements
- Bachelor’s degree or one year of Dana-Farber Associate Clinical Research Coordinator experience.
- Strong organization, communication, interpersonal, prioritization, and follow-through skills.
- Ability to work with attention to detail, discretion, and hospital confidentiality requirements.
- Computer skills, including Microsoft Office.
- Experience in a medical or scientific research setting is preferred; 0–1 years of experience is preferred.
- Some travel may be required.
Culture & Benefits
- Inclusive, diverse, and equitable environment focused on compassionate patient care.
- Work supporting cancer research, public health programs, and treatment breakthroughs.
- Collaboration with Harvard Medical School-affiliated hospitals and other research partners.
- Regular onsite work with occasional remote work.
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