Remote Clinical Research Data Coordinator II - Dallas, Tx

Overview: **The US Oncology Network** is looking for a **Remote** **Clinical Research Data Coordinator II** to join our team at **Texas Oncology**! This position will support the corporate location **Dallas, Texas****location**. This is a full\-time Monday \- Friday from 8:00am\-5:00pm with no weekends, call, or major holidays. **Must currently reside in Texas.** As a part of **The** **US Oncology Network**, **Texas Oncology** delivers high\-quality, evidence\-based care to patients close to home. **Texas Oncology** is the largest community oncology provider in the country and has approximately 600\+ providers in 300\+ sites across Texas, our founders pioneered community\-based cancer care because they believed in making the best available cancer care accessible to all communities, allowing people to fight cancer at home with the critical support of family and friends nearby. Our mission is still the same today—at Texas Oncology, we use leading\-edge technology and research to deliver high\-quality, evidence\-based cancer care to help our patients achieve “More breakthroughs. More victories.” ® in their fight against cancer. Today, **Texas Oncology** treats half of all Texans diagnosed with cancer on an annual basis. **The** **US Oncology Network** is one of the nation’s largest networks of community\-based oncology physicians dedicated to advancing cancer care in America. **The** **US Oncology Network** is supported by **McKesson** Corporation focused on empowering a vibrant and sustainable community patient care delivery system to advance the science, technology, and quality of care. ***What does the Data coordinator do?*** **The Data Coordinator,** under minimal supervision, is responsible for the collection, coordination, processing and quality control of clinical trial data. Works with clinical staff to meet data entry timelines and communicate any concerns about the data. Coordinates the scheduling of procedures, scans and monitoring and auditing visits. Provides leadership in determining and implementing improvements to policies/processes for the data team. Serves as a resource to train others regarding timely data entry and query resolution, proper conduct of sponsor monitor and audit visits. Works in compliance with US Oncology Research (USOR) Standard Operating Procedure (SOP), principles of Good Clinical Practice (GCP) and all applicable federal state and local regulations. Supports and adheres to the US Oncology Compliance Program to include the Code of Ethics and Business Standards. Responsibilities: **The essential duties and responsibilities (including but not limited to):** * Extrapolate data from source records into case report forms for all patient visits. * Ensure timely data submission in accordance with USOR SOPs. * Responsible for resolving queries, communicating concerns or questions about data to clinical staff and or research management. * Coordinates monitoring and auditing visits ensuring that all data and queries