Denver Oncology Clinical Research Data Coordinator

The US Oncology Network; Denver (CO); On-site; USD 34,000 - 41,000; Full time

Benefits offered by this job

Health, dental, and vision plans

401(k) retirement plan

PTO and holiday pay

Tuition reimbursement

Job summary

Rocky Mountain Cancer Centers in Denver is seeking an experienced Data Coordinator to support clinical research data collection, validation and management. You will ensure data quality, protocol adherence, and timely reporting while collaborating with investigators, staff and sponsors.

Responsibilities include data extraction from source records, using the trial management system, coordinating monitoring visits, and maintaining study records in a confidential manner in line with HIPAA and

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 certification 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 coordinate 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 medical terminology

Clinical trials knowledge

GCP & SOP concepts

SoCRA/ACRP certification

Education

High School Diploma

Associates Degree strongly desired

Bachelor's Degree preferred

Tools

Microsoft Office

Database management

Job description

Rocky Mountain Cancer Centers in Denver is seeking an experienced Data Coordinator to support clinical research data collection, validation and management. You will ensure data quality, protocol adherence, and timely reporting while collaborating with investigators, staff and sponsors.

Responsibilities include data extraction from source records, using the trial management system, coordinating monitoring visits, and maintaining study records in a confidential manner in line with HIPAA and