The US Oncology Network · 1 day ago
Clinical Research Coordinator
Lee, VA
Full-time
Onsite
Mid Level
3+ years expThe US Oncology Network is a leader in Cancer Care, and they are seeking a Full Time Clinical Research Coordinator for their Fairfax office. The role involves coordinating the screening, enrollment, and maintenance of patients on clinical trials, ensuring protocol compliance, and collaborating with physicians and other providers.
CommunitiesHealth CareMedicalOncologyTest and Measurement
Responsibilities
Collaborates with physicians and other providers to screen potential patients for eligibility
Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on clinical trials
Coordinates patient care in compliance with protocol requirements. Dispenses investigational drug and provides patient teaching regarding administration
Maintains investigational drug accountability. In collaboration with the physician and other providers, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings
Responsible for reviewing protocol specific billing guides and submitting billing information to appropriate personnel
Collaborates with study team on subject recruitment and study enrollment goals. Works with team to determine effective strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials
Provides clinical services as required including patient assessments. Assists with collection and maintenance of regulatory documents in accordance with USOR SOP and applicable regulations. May collaborate with Research Site Leader in the study selection process
May participate in scheduling monitoring and auditing visits as well as interact with the monitors/auditors while onsite. Participates in required training and education of staff and patients. Assists with the preparation of orders by physicians to assure that protocol compliance is maintained
Communicates with physician regarding study requirements, need for dose modification, and adverse event reporting
Qualification
Required
Associate's degree in a clinical or scientific related discipline required
Minimum three years of experience in a clinical or scientific related discipline required, preferably in oncology
Must have excellent communication skills
Excellent organizational skills
Strong ability to multi-task
Excellent time management skills
Must have strong interpersonal skills to be able to interact with multiple people on many different levels
Must have a high level of attention to detail
Must be able to work in a fast-paced environment
Preferred
Bachelor's degree preferred
Experience in oncology is preferred
SOCRA or ACRP certification preferred
Experience working with physicians preferred
Experience in Microsoft Office
Company
The US Oncology Network
Every day, The US Oncology Network helps approximately 3,300 providers deliver value-based, integrated care for patients—close to home.
10001+ employees
Funding
Current Stage
Late StageTotal Funding
unknown2010-12-30Acquired
Leadership Team
R. Steve Paulson
National Policy Board Executive Committee
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