5 дней назад
Clinical Research Coordinator II (Pediatric Oncology)
56 000 - 63 700$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Clinical Research Coordinator II (Pediatric Oncology) (Clinical Trials/Research): Coordinating pediatric oncology clinical trials from start-up and IRB submissions through data management, monitoring, patient contact, and close-out with an accent on protocol compliance, clinical data collection, and biological sample handling. Focus on preparing regulatory documentation, resolving data queries, coordinating cross-functional trial activities, and supporting audits and study monitoring.
Location: Boston, Massachusetts; hybrid work with 2–3 days onsite per week
Salary: $56,000–$63,700 per year
Company
conducts cancer research, provides patient care, educates physician-researchers, and collaborates with Harvard Medical School-affiliated hospitals.
What you will do
- Coordinate clinical trials throughout the full study lifecycle, from protocol start-up and site activation through close-out.
- Support Scientific Review Committee and IRB submissions, regulatory reporting, study documentation, and trial binder maintenance.
- Collect, manage, report, and validate clinical trial data, including source documents, case report forms, adverse events, and data queries.
- Collect, prepare, and ship protocol-related samples, including tissue samples, in accordance with trial requirements and IATA/DOT regulations.
- Collaborate with scheduling, materials management, laboratory, pharmacy, nursing, sponsors, regulatory authorities, and other research departments.
- Interact with adult and pediatric study participants, support informed consent and eligibility screening when required, and prepare for audits and monitoring visits.
Requirements
- Bachelor’s degree or two years of experience as a Dana-Farber Clinical Research Coordinator.
- 1–3 years of relevant experience, preferably in medical or scientific research or a technology-oriented business environment.
- Excellent organizational, communication, interpersonal, time-management, and prioritization skills.
- Strong attention to detail, discretion, and adherence to hospital confidentiality guidelines.
- Computer skills, including Microsoft Office.
- Ability to work in Boston with 2–3 days onsite per week and interact with patients of all ages and backgrounds.
Culture & Benefits
- Inclusive, diverse, and equitable environment focused on compassionate patient care.
- Opportunity to contribute to cancer research and public-health programs for high-risk and underserved populations.
- Work with clinical research professionals and partner institutions affiliated with Harvard Medical School.
- Responsibilities include orienting and assisting with training new staff.
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