Oncology Clinical Trial Screening Specialist

Sarah Cannon Research Institute; Nashville (TN); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Total Rewards package

Equal opportunity employer

Job summary

Sarah Cannon Research Institute (SCRI) is recruiting a Clinical Trial Central Screener to provide centralized clinical support for patient screening across its network of community-based oncology practices. The role partners with departments including Personalized Medicine and Genospace to match patients to suitable trials.

The candidate will liaise with SCRI sites, support Genospace deployment and training, and facilitate cross-functional meetings to improve screening processes.

Qualifications

• Bachelor's Degree in Nursing or RN license required.
• 3+ years as a research nurse or clinical research experience preferred.
• Must be able to read a protocol and match patients to a protocol.

Responsibilities

• Provide centralized clinical support for patient screening in SCRI's network.
• Liaise between SCRI sites and Personalized Medicine Operations to improve processes and tools.
• Assist in enhancing Genospace to improve patient-to-trial matching.
• Escalate issues to supervisor for timely resolutions.
• Support deployment, training, and use of Genospace at SCRI sites.
• Lead and facilitate routine internal and external cross-functional meetings.
• Build and maintain strategic relationships across the organization.
• Other duties as assigned.

Skills

Attention to detail

Interpersonal skills

Communication skills

Organizational skills

Team collaboration

Education

Bachelor's in Nursing

RN license

Tools

Genospace

Microsoft Excel

Microsoft Word

PowerPoint

Outlook

Job description

Sarah Cannon Research Institute (SCRI) is recruiting a Clinical Trial Central Screener to provide centralized clinical support for patient screening across its network of community-based oncology practices. The role partners with departments including Personalized Medicine and Genospace to match patients to suitable trials.

The candidate will liaise with SCRI sites, support Genospace deployment and training, and facilitate cross-functional meetings to improve screening processes.