Oncology Clinical Research Coordinator
US Oncology Network-wide Career Opportunities, Vancouver, WA, United States
Clinical Research Coordinator – Oncology
It may sound cliche, but it is true. A career taking care of cancer patients is a calling for most of us. It is more than a job. Each of us has a unique story that brought us to Compass Oncology, but those stories share common themes of care, compassion, and commitment. No matter the role each Compass team member serves, the goal is the same: to provide the best care possible for every patient.
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. 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, managing all non‑clinical aspects of the clinic trial while liaising with sponsors and monitors. While studies are conducted at all clinical sites, this position is located at our Rose Quarter Cancer Center.
Salary Range:
$28.83 – $47.18 per hour
Employment Type:
Full‑Time, 40 Hours M–F
Location:
Vancouver Cancer Center (Vancouver, WA) On‑Site
Job Scope
Under direct supervision of a physician and nurse (if applicable), responsible for enlisting, maintaining, and assuring protocol compliance for all patients on clinical trials.
Collaborates with physicians 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, including 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 times through compliance with all federal, state, and professional regulatory standards issued through OSHA and the CDC. Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
Qualifications
Education
Associate’s degree in a clinical 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
Excellent communication skills.
Excellent organizational skills.
Strong ability to multitask.
Excellent time management skills.
Strong interpersonal skills to interact with multiple people at many different levels.
High level of attention to detail.
Ability to work in a fast‑paced environment.
May be responsible for basic clinical assessments.
Benefits
Compass Oncology offers a full suite of competitive benefits that support physical, mental, and financial well‑being. For benefit‑eligible employees who work 20 hours or greater, benefits include:
Medical, Dental, Vision, Life, and Disability coverage.
HSA and Flexible Spending Accounts.
Critical Illness, Hospital, and Legal Plans.
PTO and Holiday Plans.
Retirement Savings Plans.
Robust Wellness Program and Incentives.
Employee Assistance Program.
Perks.
Physical Demands
Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye‑hand coordination. Requires standing and walking for extensive periods of time. Occasionally lifts and carries items weighing up to 40 lbs. Requires corrected vision and hearing to normal range. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Work Environment
Exposure to communicable diseases, toxic substances, ionizing radiation, medical preparations and other conditions common to an oncology/hematology clinic environment. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
EEO Statement
The US Oncology Network is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin.
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It may sound cliche, but it is true. A career taking care of cancer patients is a calling for most of us. It is more than a job. Each of us has a unique story that brought us to Compass Oncology, but those stories share common themes of care, compassion, and commitment. No matter the role each Compass team member serves, the goal is the same: to provide the best care possible for every patient.
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. 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, managing all non‑clinical aspects of the clinic trial while liaising with sponsors and monitors. While studies are conducted at all clinical sites, this position is located at our Rose Quarter Cancer Center.
Salary Range:
$28.83 – $47.18 per hour
Employment Type:
Full‑Time, 40 Hours M–F
Location:
Vancouver Cancer Center (Vancouver, WA) On‑Site
Job Scope
Under direct supervision of a physician and nurse (if applicable), responsible for enlisting, maintaining, and assuring protocol compliance for all patients on clinical trials.
Collaborates with physicians 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, including 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 times through compliance with all federal, state, and professional regulatory standards issued through OSHA and the CDC. Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
Qualifications
Education
Associate’s degree in a clinical 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
Excellent communication skills.
Excellent organizational skills.
Strong ability to multitask.
Excellent time management skills.
Strong interpersonal skills to interact with multiple people at many different levels.
High level of attention to detail.
Ability to work in a fast‑paced environment.
May be responsible for basic clinical assessments.
Benefits
Compass Oncology offers a full suite of competitive benefits that support physical, mental, and financial well‑being. For benefit‑eligible employees who work 20 hours or greater, benefits include:
Medical, Dental, Vision, Life, and Disability coverage.
HSA and Flexible Spending Accounts.
Critical Illness, Hospital, and Legal Plans.
PTO and Holiday Plans.
Retirement Savings Plans.
Robust Wellness Program and Incentives.
Employee Assistance Program.
Perks.
Physical Demands
Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye‑hand coordination. Requires standing and walking for extensive periods of time. Occasionally lifts and carries items weighing up to 40 lbs. Requires corrected vision and hearing to normal range. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Work Environment
Exposure to communicable diseases, toxic substances, ionizing radiation, medical preparations and other conditions common to an oncology/hematology clinic environment. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
EEO Statement
The US Oncology Network is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin.
#J-18808-Ljbffr