Data Coordinator

 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 click here to learn more about our research offerings.

We care about the well-being of the patients and communities we serve, and that starts with caring for our people. That’s why we have a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being. Our Total Rewards offerings serve the different needs of our diverse colleague population and ensure they are the healthiest versions of themselves. For more information regarding benefits through our parent company, McKesson, please click here.

As part of Total Rewards, we are proud to offer a competitive compensation package. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered.