Oncology Clinical Trials Coordinator

Stony Brook University; New York (NY); On-site; USD 65,000 - 80,000; Full time

Job summary

Stony Brook University in New York is seeking a Cancer Clinical Trials Study Coordinator to support administrative functions and interface with management across the hospital. The role emphasizes enrolling subjects, coordinating trials, and ensuring protocol compliance.

You will support regulatory requirements, coordinate industry-sponsored and investigator-initiated trials, review records, and assist with diverse trial activities under the PI or Cancer Clinical Trials Administrative Director.

Qualifications

• Bachelor's degree or four years of clinical/healthcare/medical industry experience.
• Three years of full-time clinical/healthcare experience.
• One year of full-time human research experience.
• Knowledge of medical terminology.

Responsibilities

• Recruit and enroll research subjects and schedule patients; attend tumor board conferences and review cancer patient reports for protocol candidates.
• Coordinate oncology clinical trials from inception to close under PI/Administrative Director; screening, eligibility, data coordination, AE reporting, and regulatory tasks.
• Plan and coordinate industry-sponsored and investigator-initiated trials, meet with sponsors, coordinate contracts and budgets.
• Respond to protocol queries and sponsor questions; educate patients and oncology staff on the research process.

Skills

Medical terminology

Clinical experience

Human research experience

Education

Bachelor's degree (foreign equivalent or higher)

Equivalent combination of clinical/healthcare experience totaling four years

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

Stony Brook University in New York is seeking a Cancer Clinical Trials Study Coordinator to support administrative functions and interface with management across the hospital. The role emphasizes enrolling subjects, coordinating trials, and ensuring protocol compliance.

You will support regulatory requirements, coordinate industry-sponsored and investigator-initiated trials, review records, and assist with diverse trial activities under the PI or Cancer Clinical Trials Administrative Director.