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Overview It may sound cliche, but it is true. A career taking care of cancer patients is a calling for most all of us. It's much more than a job. Each of us has a unique story that brought us to Compass Oncology, but those stories usually share common themes of care, compassion, and commitment. No matter the role, each Compass team member serves in, the goal is the same: to provide the best care possible for each and every one of our patients. If this sounds like you, please reach out to us. We can't wait to hear your story. Compass Oncology - Pacific Northwest's largest privately owned multi-clinic cancer care center - is looking for a Data Coordinator to join the research team. If you have the heart for service, and a team player attitude, we want to hear from you! Employment Type: Full-Time 40 Hours, M-F Location: Central Business Office (Vancouver, WA) Salary Range: $20.30- $38.73 per hour **Final offer amounts are determined by a review of the candidate's applicable experience and qualifications, as well as, internal employee equity considerations. Scope: Under general supervision is responsible for the collection, coordination, processing and quality control of clinical trial data, maintaining research protocol and other research files as applicable. Works with clinical staff to meet data entry timelines and communicate any concerns about the data. Works in compliance with US Oncology Research (USOR) Standard Operating Procedure (SOP), principles of Good Clinical Practice (GCP) and all applicable federal state and local regulations. Supports and adheres to the US Oncology Compliance Program to include the Code of Ethics and Business Standards. Responsibilities Key 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. Qualifications Education: High School Diploma required Associates Degree strongly desired; Bachelor's Degree preferred Experience/Training: 0-3 Years work experience. Medical office experience required, preferably in oncology. Experience working with Microsoft Office Experience with computer data entry and database management Experience in clinical research desired High computer literacy required. Specialized Knowledge/Skills 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 More About The Company Compass Oncology team brings together leading cancer experts in the fields of surgical, medical and radiation oncology, pathology and palliative care to provide the most comprehensive cancer care possible and an even more cohesive patient experience. In addition, the majority of our physicians specialize