Sorry, this listing is no longer accepting applications. Don’t worry, we have more awesome opportunities and internships for you.

Research Data Coordinator

United States Oncology

Research Data Coordinator

Vancouver, WA
Full Time
Paid
  • Responsibilities

    Research Data Coordinator The US Oncology Network 79 reviews - Vancouver, WA Position Summary Research Data Coordinator Clinical Trial Research is a crucial component of Compass Oncologys 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 lynch pin liaison between the on-the-ground research and the Clinical Trial Research sponsor. Compass Oncology is looking for a new member to join this hard-working team. Experience in the medical field Health Information Technologists, Medical Assistants, 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 highly preferred. If you want to be on the forefront of the newest cancer treatments, we want to hear from you! Employment Type: Full Time 40hr/week (1.0 FTE) Benefits: M/D/V, Life Ins., 401(k) Location: Vancouver, WA JOB SCOPE: Under general supervision, is responsible for the collection, coordination, processing and quality control of clinical trial data. May assist with screening patients for research protocols. Maintains research protocol information, regulatory documents and other research files as applicable. Works in compliance with US Oncology Research (USOR) Standard Operating Procedure (SOP), principles of Good Clinical Practice 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. ESSENTIAL DUTIES AND RESPONSIBILITIES: 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 processing, filing and maintaining protocol regulatory documents. May assist with 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. Maintains research records in a confidential manner according to practice policies, sponsor confidentiality agreements, HIPAA guidelines and any other applicable regulations. QUALIFICATIONS: Experience and Education: High school diploma or equivalent required; some college coursework other relevant background preferred. 1-3 years experience. Some medical office experience required, preferably in oncology. Knowledge of medical terminology required. Licenses Required: Eligibility for SoCRA certification preferred (more information at SoCRA.org) 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 in particular cancer types, bringing a heightened level of expertise to our patients. If you are a dedicated, team-oriented, patient-centered individual looking for an opportunity where you are proud of what you do, work hard, have fun, want to learn and go home at the end of the day knowing you made a difference in the lives of our patients; Compass Oncology is the place for you! As a member of The US Oncology Network, one of the nation's largest community-based cancer treatment and research networks, Compass Oncology participates in leading-edge clinical trials through US Oncology research, which has helped develop 71 FDA approved cancer therapies. We serve the Portland and Vancouver communities with six clinical offices located throughout the metro area. To learn more about Compass Oncology and its daily mission, please visit our website at www.CompassOncology.com. 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. Category: Clinical The US Oncology Network is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability or protected veteran status. 14 hours ago - save job - original job Apply On Company Site * Research Data Coordinator jobs in Vancouver, WA * Jobs at The US Oncology Network in Vancouver, WA

    • Research Data Coordinator salaries in Vancouver, WA The US Oncology Network 79 reviews US Oncology has got the backs (and the back offices) of more than 1,000 oncologists across the US. Operating as The US Oncology Network, the... Let employers find you Thousands of employers search for candidates on Indeed Upload Your Resume
  • Industry
    Other