Data Coordinator

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.

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 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. 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