Data Coordinator

Research Data Coordinator

Clinical Trial Research is a crucial component of Willamette Valley Cancer Institute's effort to provide that absolute best care available to our patients and our community. As the researchers gather data from the studies, the information needs to be extrapolated, organized, and prepared for submission to the sponsor. The Research Data Coordinator is the liaison between the on-the-ground research and the Clinical Trial Research sponsor. WVCI is looking for a new member to join this hard-working team. Experience in the medical field - Health Information Technologists, Medical Assistants, LPNs, Health Care clerical professionals - will find success in this role. Other valuable skills we are looking for include strong data entry experience and critical thinking skills. Previous experience in research is preferred.

The general pay scale for this position at WVCI is $22.00-$35.00. The actual hiring rate is dependent on many factors, including but not limited to: prior work experience, education, job/position responsibilities, location, work performance, internal equity, etc.

Employment Type: Full Time, 1.0 FTE (40 hrs/week)
Benefits: M/D/V, Life Ins., 401(k)
Location: Eugene, OR

• Extrapolates data, completes case report forms, and ensures timely data submission in accordance with USOR SOP.
• Utilizes USOR Clinical Trial Management System (CTMS) to access research forms and keeps current all applicable patient reporting and tracking functions.
• Actively prepares for and participates in monitoring and auditing activities. Assists in ensuring that all queries are resolved in a timely manner in accordance with USOR SOP and sponsor requirements.
• Responsible for reviewing CRO confirmation and follow up letters prior to filing by the Regulatory Coordinator
• May assist with pre-screening patients for potential study enrollment.
• May assist with patient scheduling for procedures required to maintain protocol compliance.
• May assist with coordinating patient follow-up visits and timely data submission.
• May assist with collection and processing of specimens, imaging documents, or other items required for research purposes.
• May assist with ordering and maintaining research supplies.
• May assist in the investigational drug accountability process.
• Uploads source documentation into the EMR and Regulatory portal
• Respond to system and/or sponsor queries
• Maintains research records in a confidential manner according to practice policies, sponsor confidentiality agreements, HIPAA guidelines and any other applicable regulations.
• Other duties as assigned.

• High school diploma or equivalent required; some college coursework other relevant background preferred.
• 1-3 years of medical experience, preferable in Oncology
• Knowledge of medical terminology preferred.

PHYSICAL DEMANDS:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Physical demands of this job typically require full range of body motion including manual and finger dexterity and eye-hand coordination and the ability to read and note appropriate measurements. Requires sitting/standing for extensive periods of time. Occasionally lifts and carries items weighing up to 40 lbs. Requires corrected vision and hearing to normal range. While performing the duties of this job, the employee is regularly exposed to direct contact with patients with potential for exposure to toxic substances, medicinal preparations, and chemotherapeutic agents.

The US Oncology Network is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin.