Site Regulatory/ 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. The primary responsibility of the **Site Data and Regulatory Coordinator** is providing support to the Clinical Research Coordinator (CRC) and Research Nurse daily, ensuring all activities are conducted according to company standard operating procedures (SOPs) and all applicable Good Clinical Practice (GCP) and ICH regulations and guidelines. In addition, managing and tracking regulatory documents and protocol training to maintain site compliance for industry sponsors and GCP/FDA requirements and ensuring Regulatory paper documents are printed and electronically filed, in preparation for monitoring visits. This position will work closely with the regulatory affairs department, site leadership and/or principle investigators to ensure compliance as well as preparing for auditing activities while meeting strict deadlines. - You will enter data into study specific case report forms or electronic data capture systems for each assigned clinical trial. - You will resolve queries for in electronic data capture systems for each assigned clinical trials. - You will work with the Clinical Research Coordinator to meet industry trial data deadlines. - You will establish an effective workflow with the Clinical Research Coordinator to effectively manage clinical trials. - You will obtain source documentation for patients enrolled into clinical trials. - Assist in SAE reporting and tracking. - You will create and maintain patient visit tracking spreadsheets. - You will create imaging requests, manages imaging tracker, answers queries, and uploads images per imaging guidelines for assigned clinical trials. - You will establish and maintain positive relationship with Clinical Research Associates (CRA) - You will investigate and report protocol deviations, when applicable - You will maintain and archive study administrative files. - You will maintain assigned closed to accrual trials. - You will report required metrics to leadership team. - You will attend all SIVs for assigned trials. - You will schedule and manage monitor visits including resolution of follow up items. - You will assist other colleagues as requested and performs other related work as needed. - You will provide site level regulatory support to the site in relation to the status of start-up and ongoing regulatory maintenance - You will establish and maintain a document management system for regulatory paper and electronic files for each study at the site - You will escort monitors to and from the secured Monitoring Suite area - You will maintain updated physician credentials and other critical documentation ensuring compliance - You will meet with monitors, study sponsor representatives and auditors as requested - You will track documents pending site regulatory signatures - You will route and track completion of protocol training - You will maintain FDA and GCP required regulatory documentation for individual site, studies, sponsors and/or other networks. Ensures all regulatory documentation is compliant with local Standard Operati…