Clinical Trials Data Coordinator — Cancer Research

McKesson

United States

On-site

USD 32,000 - 37,000

Full time

14 days+
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Job summary

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, is seeking a Data Coordinator to support Study Coordinators in clinical trials. You will ensure data deadlines are met, obtain source documents, and assist with CRF completion and SAE tracking.

The role emphasizes adherence to SCRI SOPs, GCP and ICH guidelines, with duties spanning data operations and study file maintenance. Bachelor’s degree preferred; healthcare or trial support experience is a plus.

Qualifications

  • Knowledge of scientific, medical, and regulatory terms.
  • Knowledge of GCP and GMP.
  • Detail-oriented.
  • Excellent English written and oral skills.
  • Bachelor’s degree preferred.
  • Healthcare experience, clinical trials support, or pharmaceutical industry experience preferred.

Responsibilities

  • Support Study Coordinators to meet trial data deadlines.
  • Obtain source documentation for patients enrolled into trials.
  • Assist with case report form completion and query resolution.
  • Assist in SAE reporting and tracking.
  • Create and maintain patient visit tracking spreadsheets.
  • Maintain and archive study administrative files.
  • Contribute to special procedural projects to improve Drug Development Data Operations.
  • Monitor adherence to SCRI SOPs, GCP, and ICH guidelines throughout trials.

Skills

GCP/GMP knowledge
Attention to detail
Excellent English (written/spoken)
Healthcare experience

Education

Bachelor’s degree preferred

Job description

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, is seeking a Data Coordinator to support Study Coordinators in clinical trials. You will ensure data deadlines are met, obtain source documents, and assist with CRF completion and SAE tracking.

The role emphasizes adherence to SCRI SOPs, GCP and ICH guidelines, with duties spanning data operations and study file maintenance. Bachelor’s degree preferred; healthcare or trial support experience is a plus.

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