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The US Oncology Network

Supports independent oncology practices, patient care

Research Data Coordinator

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeDenver, CO, USA

About the Job

Requirements

  • A high school diploma is required.
  • A bachelor's degree is preferred, and an associate degree is strongly desired.
  • At least 3 years of medical office experience, preferably in oncology, is required.
  • At least 3 years of experience as a data coordinator is required.
  • Advanced experience with Microsoft Office is required.
  • Advanced experience with computer data entry and database management is required.
  • Hazmat/IATA training is required.
  • Advanced knowledge of oncology medical terminology is required.
  • Advanced knowledge of clinical trials, regulatory processes, Good Clinical Practice, and Standard Operating Procedure concepts is required.
  • Candidates must pass a background check and non-federal drug test after an offer and before hire.
  • Candidates must provide proof of influenza vaccination upon commencing employment; reasonable accommodation for exemptions may be considered case by case.

Responsibilities

  • Collect, validate, and manage clinical research data to support study objectives and regulatory requirements.
  • Extrapolate data from source records into case report forms for all patient visits and submit data in a timely manner according to USOR Standard Operating Procedures.
  • Resolve data queries and communicate data concerns or questions to clinical staff and research management.
  • Use the USOR clinical trial management system to access research forms and maintain applicable patient reporting and tracking functions, including subject case report form binders and folders.
  • Coordinate patient billing and research payout or payment tracking when assigned.
  • Maintain confidential research records according to practice policies, sponsor confidentiality agreements, HIPAA guidelines, and applicable regulations.
  • Coordinate monitoring and auditing visits, ensuring data and queries are entered and resolved according to USOR and sponsor requirements.
  • Assist with investigational drug accountability, ordering, and maintaining research supplies.
  • Schedule patient follow-up appointments and procedures needed to maintain protocol compliance.
  • Collect and process specimens, imaging documents, and other items required for research purposes.
  • Provide training and education to other data coordinators at the site.

Desired Qualifications

  • SoCRA or ACRP certification is preferred.

About the Company

The US Oncology Network

Supports independent oncology practices, patient care

The US Oncology Network coordinates a nationwide group of independent oncology practices to deliver cancer care close to home. It provides local physicians with clinical and business support, including access to advanced technologies and shared resources, so they can offer comprehensive, value-based treatment in community settings. By pooling expertise and capabilities, the Network helps independent practices operate more efficiently and sustainably while maintaining physician autonomy. Its goal is to improve patient outcomes and physician satisfaction by delivering high-quality, patient-centered care through a scalable, practice-centric platform.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Upper Merion Township, Pennsylvania
Founded
1999

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