Oncology Clinical Research Coordinator

The US Oncology Network•Vancouver, WA

21h•Onsite

About The Position

Compass Oncology is seeking a full-time Clinical Research Coordinator (CRC) to join their team. Clinical research is a major service offered through Compass Oncology and The US Oncology Network. CRCs are responsible for enlisting, maintaining, and assuring protocol compliance for all patients on clinical trials. They collaborate with Physicians, other clinical staff, and members of the research department to manage all non-clinical aspects of the clinic trial and liaise with study Sponsors and Monitors. This position will be located at our Rose Quarter Cancer Center.

Requirements

Associates Degree in a clinical or scientific related discipline required.
Minimum one year 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.
May be responsible for basic clinical assessments.

Nice To Haves

Bachelor's degree preferred.
Experience working with physicians preferred.

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 protocol.
Coordinates patient care in compliance with protocol requirements.
May disburse investigational drug and provide patient teaching regarding administration.
Maintains investigational drug accountability.
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.
Responsible for accurate and timely data collection, documentation, entry, and reporting.
Schedules and participates in monitoring and auditing activities.
Maintains regulatory documents in accordance with USOR SOP and applicable regulations.
Participates in required training and education programs.
Responsible for education of clinic staff regarding clinical research.
May collaborate with Research Site Leader in the study selection process.
Additional responsibilities may include working directly with other (non-USOR) research bases and/or sponsors.
Provides a safe environment for patients, families, and clinical staff at all time through compliance with all federal, state, and professional regulatory standards as issued through OSHA and the CDC.
Maintains strict patient confidentiality according to HIPAA regulations and applicable law.