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The US Oncology Network · 5 hours ago

Clinical Research Coordinator II (Frederick/Germantown)

Frederick, MD

Full-time

Onsite

Mid Level

$59K/yr - $77K/yr

3+ years exp

The US Oncology Network is seeking a Clinical Research Coordinator II to join their Maryland Oncology Hematology team, dedicated to providing exceptional cancer care. This role involves recruiting and enrolling patients in clinical trials, ensuring protocol compliance, and coordinating patient care in collaboration with physicians.

CommunitiesHealth CareMedicalOncologyTest and Measurement

Responsibilities

Screens potential patients for protocol 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. May disburse investigational drug. Maintains investigational drug accountability. Oversees the preparation of orders by physicians to assure that protocol compliance is maintained. Packages and ships lab specimens to central vendors where applicable. Required to complete Hazmat and/or IATA training

In collaboration with the physician, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings and participates in data collection of all subjects

Responsible for preparing study-related documentation such as protocol worksheets, adverse event reports, institutional review board documents, and annual continuing review reports

Maintains regulatory documents in accordance with USOR SOP and applicable regulations. May participate in scheduling monitoring and auditing visits, as well as interact with the monitors/auditors while onsite. May collaborate with Research Site Leader in the study selection process

Participates in required training and education programs. May be responsible for education of clinic staff regarding clinical research. Collaborates with staff in the development of action plans and performance improvement opportunities with staff to improve quality

May be responsible for compiling and reporting protocol activity, accrual trends, data entry compliance, and research financial information to practice administration and physicians. May be responsible for reviewing protocol specific billing guides and submitting billing information to appropriate personnel

Qualification

Clinical research experienceSoCRAACRP certificationMicrosoft OfficeOncology experienceMulti-taskingPatient-facing experienceCommunication skillsOrganizational skillsTime managementInterpersonal skillsAttention to detailSelf-motivated

Required

Associate's degree in a clinical or scientific related discipline required, Bachelor's degree preferred

Minimum three years of experience in a clinical or scientific related discipline required, preferably in oncology

Experience in Microsoft Office

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

The successful candidate will demonstrate extensive experience in patient-facing roles, maintaining a professional and empathetic demeanor while delivering high-quality care

This position requires a self-motivated individual who can work independently and manage priorities effectively in a fast-paced environment