Clinical Research Coordinator - Float

Location: Portland

Overview

It may sound cliché, but it is true. A career taking care of cancer patients is a calling for most all of us. It's much more than a job. Each of us has a unique story that brought us to Compass Oncology, but those stories usually share common themes of care, compassion, and commitment. No matter the role each Compass team member serves in, the goal is the same: to provide the best care possible for each and every one of our patients.

We have an exciting opportunity for a full-time Clinical Research Coordinator (CRC). Clinical research is a major service offered through Compass Oncology and The US Oncology Network. Our CRC's are responsible for enlisting, maintaining, and assuring protocol compliance for all patients on clinical trials. Collaborating with Physicians, other clinical staff, and members of the research department, the CRC's help to manage all non-clinical aspects of the clinic trial as well as liaising with the Sponsors and Monitors of the study.

While studies are conducted at all clinical sites, this position will be located at our Rose Quarter Cancer Center.

Employment Type:

Part-Time, 20 Hours

Location:

West Cancer Center (Tigard, OR) On-Site

Salary Range: $25.49 - $47.18 per hour

Final offer amounts are determined by a review of the candidate's applicable experience and qualifications, as well as, internal employee equity considerations.

JOB SCOPE:

Under direct supervision of a physician and nurse (if applicable), is responsible for enlisting, maintaining, and assuring protocol compliance for all patients on clinical trials. Collaborates with physician in determining eligibility of patients for clinical trials. Provides education to staff and patients. Ensures site research quality by practicing in compliance with US Oncology Research, Inc. (USOR) Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations.

Supports and adheres to US Oncology Compliance Program, to include the Code of Ethics Business Standards.

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.

Qualifications

Education:

* Associates Degree in a clinicial or scientific related discipline required, Bachelor's degree preferred.

* Minimum one year of experience in a clinical or scientific related discipline required, preferably in oncology.

Business/Training:

* Experience in Microsoft Office

* Experience working with physicians preferred.

Specialized Knowledge/

Skills:

* Must have excellent communication skills.

* Excellent organizational skills.

* Strong ability to multi-taks.

* Excellent time management skills.

* Must have strong interpersonal skills to be able to interact with mulitple 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.

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!

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