Clinical Trial Central Screener: Drive Precision Oncology

Sarah Cannon Research Institute

Tennessee

On-site

USD 60,000 - 80,000

Full time

8 days ago

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Job summary

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, seeks a Clinical Trial Central Screener to provide centralized clinical support for patient screening across SCRI’s network of community-based oncology practices.

You will collaborate with Precision Medicine, Genospace, Therapeutic Development and Research Operations to identify patients for trials, perform remote chart reviews for clinical suitability, and communicate with site personnel when eligible candidates are found.

Qualifications

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

Responsibilities

  • Provide centralized clinical support for the patient screening process.
  • Act as liaison between SCRI network sites and internal teams to refine processes and tools.
  • Assist in enhancing Genospace to improve trial matching.
  • Escalate issues to supervisor to ensure timely resolution during screening.
  • 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.

Skills

Attention to detail
Communication skills
FDA Regulations
ICH Guidelines
Collaboration

Education

Bachelor's Degree in Nursing
Licensed Registered Nurse

Tools

Genospace

Job description

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, seeks a Clinical Trial Central Screener to provide centralized clinical support for patient screening across SCRI’s network of community-based oncology practices.

You will collaborate with Precision Medicine, Genospace, Therapeutic Development and Research Operations to identify patients for trials, perform remote chart reviews for clinical suitability, and communicate with site personnel when eligible candidates are found.

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