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Sarah Cannon Research Institute

Community-based oncology clinical research organization

Source Document Specialist

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeNashville, TN, USAIn-person

About the Job

Requirements

  • An associate degree is required; a bachelor's degree is preferred.
  • At least 2 years of experience working in a health care organization; oncology experience is preferred.
  • Knowledge of scientific, medical, and regulatory terms.
  • Knowledge of Good Clinical Practice and Good Manufacturing Practice.
  • Excellent written and oral English skills.

Responsibilities

  • Support the Study Coordinator in meeting industry trial data deadlines.
  • Obtain source documentation for patients enrolled in clinical trials.
  • Assist the Study Coordinator with case report form completion and query resolution as needed.
  • Assist the Study Coordinator in obtaining medical records, including research charts.
  • Create and maintain spreadsheets for medical record and research chart accountability.
  • Maintain and archive study administrative files.
  • Work with Tennessee Oncology medical record departments to ensure accountability of records.
  • Work with Iron Mountain to locate archived records.
  • Meet regularly with the project manager.
  • Assess adherence to Sarah Cannon standard operating procedures, Good Clinical Practice, and International Council for Harmonisation regulations and guidelines.

Desired Qualifications

  • Oncology experience.
  • Healthcare experience, clinical trials support, or pharmaceutical industry experience.

About the Company

Sarah Cannon Research Institute

Community-based oncology clinical research organization

Sarah Cannon Research Institute (SCRI) is a global oncology research organization that conducts cancer clinical trials in community settings, partnering with pharmaceutical and biotech sponsors, physicians, and patients to develop new treatments. It works as an oncology-focused contract research organization (CRO) and centralized site management organization (SMO), running trials across more than 200 locations with roughly 1,500 research physicians, and applies technology such as its Accelero platform to personalized-medicine studies. Over more than 30 years it has completed more than 900 first-in-human trials across early- to late-phase research. What sets SCRI apart is this community-based model paired with early-phase depth, which has helped advance most new cancer therapies the FDA approved in the past decade. The goal is to accelerate oncology research from early trials to approval and bring advanced cancer treatments to patients.

Company size
1-10
Company stage
Not listed
Total funding
Not listed
Headquarters
Beach Haven, NJ
Founded
Not listed

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