The US Oncology Network
Clinical Research Coordinator II (Frederick/Germantown)
The US Oncology Network, Frederick, Maryland, United States, 21701
Clinical Research Coordinator II (Frederick/Germantown)
Overview
Join Our Team at Maryland Oncology Hematology! We’re seeking passionate and talented professionals to provide exceptional cancer care. With 15+ locations across Maryland and DC, we offer a dynamic and supportive environment where you can grow and thrive.
Salary : $58,798 – $77,435 (dependent on experience, education, and responsibilities).
Job Profile Summary
Responsible for recruiting, screening, consenting, and enrolling patients in clinical trials. Coordinates and oversees patient visits in accordance with protocol requirements, ensuring compliance and maintaining high standards of patient care and data integrity.
Key Responsibilities
Screen potential patients for protocol eligibility and present trial concepts.
Coordinate patient care to ensure protocol compliance, including investigational drug accountability and order preparation oversight.
Collaborate with physicians to review patient status, adverse events, concomitant medications, and protocol compliance.
Prepare study‑related documentation such as protocol worksheets, adverse event reports, IRB documents, and continuing review reports.
Maintain regulatory documents per USOR SOP and applicable regulations; assist with monitoring and auditing visits.
Provide required training and education to clinic staff and participate in performance improvement initiatives.
Compile and report protocol activity, accrual trends, data entry compliance, and financial information to practice administration and physicians.
Qualifications
Education
Associate’s degree in a clinical or scientific discipline required; Bachelor’s degree preferred.
Minimum three years of experience in a clinical or scientific discipline, preferably in oncology.
SoCRA or ACRP certification preferred.
Business Experience
Experience with Microsoft Office.
Preferred experience working with physicians.
Preferred experience in clinical research.
Specialized Knowledge/Skills
Excellent communication, organizational, interpersonal, and time‑management skills.
Strong multitasking abilities and high attention to detail.
Capacity to work in a fast‑paced environment.
Basic clinical assessment skills (preferred).
Working Conditions
Environment: Traditional office environment within an oncology/hematology clinic. Physical requirements include extensive computer work, standing and walking for long periods, and occasional lifting of up to 40 lbs. Reasonable accommodations will be provided to enable employees with disabilities to perform essential functions.
(This description is general in nature and is not intended to be an exhaustive list of all responsibilities. Other duties may be assigned as needed.)
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Join Our Team at Maryland Oncology Hematology! We’re seeking passionate and talented professionals to provide exceptional cancer care. With 15+ locations across Maryland and DC, we offer a dynamic and supportive environment where you can grow and thrive.
Salary : $58,798 – $77,435 (dependent on experience, education, and responsibilities).
Job Profile Summary
Responsible for recruiting, screening, consenting, and enrolling patients in clinical trials. Coordinates and oversees patient visits in accordance with protocol requirements, ensuring compliance and maintaining high standards of patient care and data integrity.
Key Responsibilities
Screen potential patients for protocol eligibility and present trial concepts.
Coordinate patient care to ensure protocol compliance, including investigational drug accountability and order preparation oversight.
Collaborate with physicians to review patient status, adverse events, concomitant medications, and protocol compliance.
Prepare study‑related documentation such as protocol worksheets, adverse event reports, IRB documents, and continuing review reports.
Maintain regulatory documents per USOR SOP and applicable regulations; assist with monitoring and auditing visits.
Provide required training and education to clinic staff and participate in performance improvement initiatives.
Compile and report protocol activity, accrual trends, data entry compliance, and financial information to practice administration and physicians.
Qualifications
Education
Associate’s degree in a clinical or scientific discipline required; Bachelor’s degree preferred.
Minimum three years of experience in a clinical or scientific discipline, preferably in oncology.
SoCRA or ACRP certification preferred.
Business Experience
Experience with Microsoft Office.
Preferred experience working with physicians.
Preferred experience in clinical research.
Specialized Knowledge/Skills
Excellent communication, organizational, interpersonal, and time‑management skills.
Strong multitasking abilities and high attention to detail.
Capacity to work in a fast‑paced environment.
Basic clinical assessment skills (preferred).
Working Conditions
Environment: Traditional office environment within an oncology/hematology clinic. Physical requirements include extensive computer work, standing and walking for long periods, and occasional lifting of up to 40 lbs. Reasonable accommodations will be provided to enable employees with disabilities to perform essential functions.
(This description is general in nature and is not intended to be an exhaustive list of all responsibilities. Other duties may be assigned as needed.)
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