Research Data Specialist - Breast Oncology Clinical Trials (Clinical Research)
Контакты
50 500 - 56 700$
Формат работы
hybrid
Тип работы
fulltime
Грейд
junior
Английский
b2
Страна
US
qamicrosoft officedata managementoncologyclinical researchclinical trialsmedical records
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
Очень мало
$51к-57к/год
$68к$82кмедиана$110к
По похожим ролям (43) ~ $82к/год
68
Хорошая вакансия
развернуть
Понятная стартовая позиция в известном онкологическом исследовательском центре дает полезный опыт клинических исследований, но удаленная работа доступна только из Новой Англии, а обязанности зависят от программы.
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Оплата ниже рынкаУдаленка с ограничениемПодходит для стартаЗначимая область
Оценка от Hirify AI
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Research Data Specialist - Breast Oncology Clinical Trials (Clinical Research): Collecting, managing, abstracting, and quality-checking patient clinical data for breast oncology clinical trials with an accent on medical record review, database organization, and clinical research documentation. Focus on entering accurate data within trial timelines, monitoring patient status, supporting case report forms, and collaborating with clinical research and information services staff.
Location: Fully remote from Maine, Vermont, New Hampshire, Massachusetts, Connecticut, or Rhode Island, with occasional onsite time in Boston, Massachusetts.
Salary: $50,500–$56,700 per year.
Company
hirify.global conducts cancer research, provides patient care, educates physician-researchers, and advances treatment through clinical and public health programs.
What you will do
Review and abstract medical records for patients participating in assigned clinical trials.
Collect, enter, manage, and quality-check clinical data in relevant databases and clinical research information systems.
Monitor patient status, trial eligibility, data completeness, and submission timelines.
Support the development, testing, and implementation of case report forms for investigator-initiated trials.
Collaborate with principal investigators, physicians, clinic staff, and Information Services on data collection and reporting needs.
Depending on the program, support patient consenting, biological specimen tracking, regulatory files, outcomes reporting, audits, and data reports.
Requirements
Bachelor’s degree or one year of experience as a Dana-Farber Associate Research Data Specialist.
Excellent organizational and communication skills.
Strong interpersonal skills and the ability to interact effectively with staff at all levels and external contacts.
Strong attention to detail and the ability to manage time and prioritize workload.
Ability to maintain discretion and follow institutional confidentiality guidelines.
Computer skills, including Microsoft Office.
Patient contact is required and includes patients of all ages.
Nice to have
0–1 year of experience in a medical, scientific research, or technology-oriented business environment.
Culture & Benefits
Fully remote work is available from an eligible New England state, with occasional onsite time in Boston.
Work in an innovative, caring, inclusive, diverse, and equitable environment.
Contribute to cancer research, patient care, and programs serving high-risk and underserved populations.
Collaborate with Harvard Medical School-affiliated hospitals and other research partners.
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