You will assist the Study Coordinator with query resolution if needed.
You will assist the Study Coordinator to obtain medical record including research chart.
You will create and maintain spreadsheet for medical record and research chart accountability.
You will maintain and archive study administrative files.
You will work closely with Tennessee Oncology medical record departments to assure accountability of records.
You will work closely with Iron Mountain to locate archived records.
You will meet with project manager on a regular basis.
You will assess adherence to Sarah Cannon SOPS, Good Clinical Practice (GCP) and ICH regulations and guidelines.
What you should have for this role
An Associate Degree; Bachelor Degree preferred
At least 2 years of experience working in health care organization – oncology preferred
Knowledge of scientific, medical, and regulatory terms
Knowledge of GCP and Good Manufacturing Practice (GMP)
Detail-oriented
Excellent English written and oral skills.
Healthcare experience, Clinical trials support, or pharmaceutical industry experience preferred
About Sarah Cannon Research Institute
Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials. Focused on advancing therapies for patients over the last three decades, SCRI is a leader in drug development. In 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country. It has conducted more than 850 first-in-human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA in the past decade. SCRI’s research network brings together more than 1,300 physicians who are enrolling patients into clinical trials at more than 200 locations in 20+ states across the U.S. Please click here to learn more about our research offerings.
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