Oncology Research Data Coordinator

Us Oncology Inc; Denver (CO); On-site; USD 34,000 - 41,000; Full time

Benefits offered by this job

Health, dental, and vision plans

Wellness program

Health savings account (HSA)

Flexible spending accounts (FSA)

Research bonus based on department

401(k) retirement plan

Life insurance

Short-term disability insurance

Long-term disability insurance

Employee Assistance Program

PTO, holiday pay

Tuition reimbursement

Employee paid critical illness and/or;

Job summary

Rocky Mountain Cancer Centers in Denver is seeking an experienced Research Data Coordinator to ensure accurate collection, validation, and management of clinical research data in support of study objectives and regulatory requirements.

The role collaborates with investigators, research staff, and sponsors to maintain data quality, protocol adherence, and timely reporting, contributing to patient care and clinical research initiatives. Hourly pay $25.00-$30.00, with competitive benefits.

Qualifications

• High School Diploma required.
• Associates Degree strongly desired, Bachelor's Degree preferred.
• Minimum 3 years medical office experience (preferably oncology).
• Minimum 3 years as Data Coordinator required.
• SoCRA or ACRP cert. preferred.

Responsibilities

• Extrapolate data from source records into case report forms for all patient visits. Ensure timely data submission in accordance with USOR SOPs.
• 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.
• May be responsible for coordinating patient billing and research payout/payment tracking.
• Maintains research records in a confidential manner according to practice policies, sponsor confidentiality agreements, HIPAA guidelines and any other applicable regulations.
• Coordinates monitoring and auditing visits ensuring that all data and queries are entered and resolved in accordance with the USOR and sponsor requirements.
• Assists with investigational drug accountability process, ordering and maintaining research supplies.
• Schedules patient follow up appointments and/or procedures required to maintain protocol compliance.
• Collecting and processing of specimens, imaging documents and other items required for research purposes.
• Acts as resource for other for training and education of other data coordinators at the site/location.

Skills

Advanced knowledge of medical terms (c

Clinical trials, regulatory processes,

Education

High School Diploma

Associates Degree

Tools

Microsoft Office

Database management

Job description

Rocky Mountain Cancer Centers in Denver is seeking an experienced Research Data Coordinator to ensure accurate collection, validation, and management of clinical research data in support of study objectives and regulatory requirements.

The role collaborates with investigators, research staff, and sponsors to maintain data quality, protocol adherence, and timely reporting, contributing to patient care and clinical research initiatives. Hourly pay $25.00-$30.00, with competitive benefits.