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Data Coordinator

Job in Nashville, Davidson County, Tennessee, 37247, USA
Listing for: McKesson’s Corporate
Full Time position
Listed on 2026-02-01
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

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It’s More Than a Career, It’s a Mission.

Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day.

Our Mission

People who live with cancer – those who work to prevent it, fight it, and survive it – are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the world.

The Data Coordinator provides support to Study Coordinator on a daily basis, ensures all activities are conducted according to company standard operating procedures (SOPs) and all applicable Good Clinical Practice (GCP) and ICH regulations and guidelines.

You will support the Study Coordinator to meet industry trial data deadlines

You will obtain source documentation for patients enrolled into clinical trial

You will assist the Study Coordinator with case report form completion and query resolution

You will assist in Serious Adverse Event (SAE) reporting and tracking

You will create and maintain patient visit tracking spreadsheets for the Study Coordinator

You will maintain and archive study administrative files

You will be assigned special procedural projects to enhance the functioning of Drug Development Data Operations

Throughout the conduct of the clinical trial you will assess adherence to SCRI SOPS, Good Clinical Practice (GCP) and ICH regulations and guidelines

What you should have for this role:

Knowledge of scientific, medical, and regulatory terms

Knowledge of GCP and Good Manufacturing Practice (GMP)

Detail-oriented

Excellent English written and oral skills.

Bachelor Degree preferred.

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 750 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 today.

SCRI’s research network brings together more than 1,300 physicians who are actively enrolling patients into clinical trials at more than 250 locations in 24 states across the U.S. Please  to learn more about our research offerings.

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