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. 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. Data Coordinator The Data Coordinator provides support to the Clinical Research Coordinator (CRC) and Research Nurse on a daily basis, ensuring all activities are conducted according to company standard operating procedures (SOPs) and all applicable Good Clinical Practice (GCP) and ICH regulations and guidelines. Responsibilities Support CRC to meet industry trial data deadlines. Obtain source documentation for patients enrolled onto clinical trials. Assist CRC with case report form completion and query resolution. Assist in Serious Adverse Event (SAE) reporting and tracking. Create and maintain patient visit tracking spreadsheets for CTS. Maintain and archive study administrative files. Maintain and archive regulatory files. Assist in ensuring source document templates are accurate. Be assigned special procedural projects to enhance the functioning of the research program. Assess adherence to SCRI SOPs, Good Clinical Practice (GCP) and ICH regulations and guidelines throughout clinical trial conduct. 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. Compensation $24/hr - $27/hr Benefits Our Total Rewards package includes comprehensive benefits to support physical, mental, and financial well-being. 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. We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. #J-18808-Ljbffr