Data Coordinator Sr.- Dallas Sammons- Remote

The US Oncology Network•Dallas, TX

7d•Remote

About The Position

Texas Oncology is looking for a Data Coordinator to join our team! This position will support the Dallas Sammons location. This is a Remote position. Typical hours are Mon-Fri from 8am-5pm. This position can be either a level 1, 2 or Sr based on experience. Texas Oncology is the largest community oncology provider in the country and has approximately 600+ providers in 220+ sites across Texas and southeastern Oklahoma. 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, high-touch, 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.

Requirements

High School Diploma required
Medical terminology required
Minimum 7 years as a Data Coordinator required.
Experience in Microsoft Office
Experience with computer data entry and database management
High computer literacy required
Excellent written and oral communication skills
Excellent multi-tasking skills
High attention to detail and accuracy
Ability to independently organize, prioritize, and make decisions
Knowledgeable of medical terminology

Nice To Haves

Associates Degree strongly desired
Bachelor's Degree preferred
Some medical office experience required; preferably oncology
Minimum 3 years medical office experience (preferably oncology)
Minimum 3 years as Data Coordinator required
SoCRA or ACRP cert. preferred
Experience in clinical research desired

Responsibilities

Extrapolate data from source records into case report forms for all patient visits and 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.
Utilizes USOR clinical trial management system to access research forms and keep current all applicable patient reporting and tracking functions including but not limited to subject CRF Binders/Folders.
Maintains research records in a confidential manner according to practice policies sponsor confidentiality agreements, HIPAA guidelines and any other applicable regulations.
Actively participates in sponsor monitoring and auditing visits, ensuring that all data and queries are entered and resolved in accordance with USOR and sponsor requirements.
Assist with ordering and maintaining research supplies.
Assist with scheduling patient follow up appointments and/or procedures required to maintain protocol compliance.
Assist with collecting and processing of specimens, imaging documents, and other items required for research purposes.