13 часов назад
Senior Clinical Research Coordinator (Clinical Research)
73 600 - 83 000$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Clinical Research Coordinator (Clinical Research): Coordinating clinical trials at the Dana-Farber Milford Satellite location with an accent on protocol execution, patient data management, regulatory submissions, and study compliance. Focus on managing trials throughout their life cycle, collecting and shipping protocol samples, resolving data queries, and preparing for audits and monitoring visits.
Location: Onsite at the Milford Satellite location with up to one remote day per week; remote work is limited to New England states (ME, VT, NH, MA, CT, RI).
Salary: $73,600–$83,000 per year
Company
conducts cancer research, delivers patient care, educates physician-researchers, and advances treatment through partnerships with Harvard Medical School-affiliated hospitals.
What you will do
- Coordinate clinical trials from protocol receipt and start-up through site activation, ongoing conduct, and close-out.
- Collect, manage, and report clinical data, source documents, case report forms, adverse events, and data queries.
- Prepare regulatory documentation and IRB submissions while maintaining participant and regulatory binders.
- Collect, prepare, and ship tissue and other study samples according to protocol and IATA/DOT requirements.
- Coordinate with research, pharmacy, laboratory, materials management, scheduling, and nursing departments.
- Interact with participants, sponsors, regulatory authorities, auditors, and monitoring teams.
Requirements
- Bachelor’s degree or three years of Dana-Farber Clinical Research Coordinator experience.
- Three to five years of equivalent experience.
- Understanding of ICH/GCP, federal regulations, DF/HCC SOPs, research design, and clinical research department responsibilities.
- Ability to coordinate PI-initiated multicenter studies and support, train, and educate CRC I and II staff.
- Strong organization, communication, interpersonal, prioritization, follow-through, and attention-to-detail skills.
- Computer proficiency, including Microsoft Office, and adherence to confidentiality guidelines.
Nice to have
- Experience in a medical or scientific research setting or a comparable technology-oriented business environment.
Culture & Benefits
- Inclusive, diverse, and equitable environment focused on compassionate patient care.
- Work with research, clinical, and academic partners on programs designed to advance cancer treatment.
- Patient contact includes adults of all ages and populations.
- Schedule includes onsite work with limited weekly remote flexibility from an eligible New England state.
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