2 дня назад
Clinical Research Coordinator II - Foxborough
56 000 - 62 700$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Clinical Research Coordinator II - Foxborough (Clinical Trials): Coordinating clinical trials across Dana-Farber satellite sites with an accent on regulatory compliance, patient data management, protocol sample handling, and study documentation. Focus on preparing IRB submissions, resolving data queries, supporting audits and monitoring visits, and coordinating study activities across onsite locations.
Location: Foxborough, Massachusetts, United States; onsite work with occasional remote support. Travel to the Longwood campus and other Dana-Farber satellite sites may be required.
Salary: $56,000–$62,700 per year.
Company
conducts cancer research, clinical trials, and patient care in collaboration with Harvard Medical School-affiliated hospitals.
What you will do
- Coordinate clinical trials and site activation activities across Dana-Farber satellite locations.
- Collect, manage, and report patient clinical data using source documents and case report forms.
- Prepare regulatory reports and IRB submissions while maintaining study binders and tracking databases.
- Coordinate protocol sample collection, preparation, and shipment in accordance with IATA/DOT requirements.
- Prepare for audits and monitoring visits, resolve data queries, and support study close-out activities.
- Communicate with lead study teams, sponsors, regulatory authorities, study participants, and internal departments.
Requirements
- Bachelor’s degree.
- 1–3 years of related experience preferred, ideally in a medical or scientific research setting.
- Understanding of clinical research coordination, clinical trial phases, ICH/GCP, federal regulations, and DF/HCC SOPs.
- Knowledge of CRF completion, accurate data transcription, adverse event reporting, and regulatory documentation.
- Ability to work independently across satellite locations and provide onsite and remote support.
- Strong organizational, communication, interpersonal, prioritization, and follow-through skills; Microsoft Office proficiency required.
Culture & Benefits
- Work in an innovative, inclusive, and equitable cancer research and patient care environment.
- Minimal patient contact.
- Opportunity to orient and assist in training new staff.
- Role includes onsite work with occasional remote support and travel between research locations.
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