TI Sr Clinical Research Assistant; Clinical Research Coordinator

TI Sr Clinical Research Assistant (Clinical Research Coordinator)

Location:

US-OR-Portland

Requisition :

Position Category: Research

Job Type: Research

Position Type: Regular Full-Time

Posting Salary Range: $50,128 - $75,171.20 per year with offer based on experience, education and internal equity

HR Mission: School of Medicine

Drug Testable: Yes

The mission of the Knight Clinical Research Management organization is to support the conduct of translational clinical research aimed at improving the lives of people and families with cancer by applying innovative strategies for cancer prevention, screening, diagnosis and treatment. The support is provided through proactive, high quality and efficient study management in compliance with federal regulations and local policies and procedures.

This fast‑paced and highly intense research environment requires management of complex therapeutic interventional (TI) trials and clinical research studies involving a very vulnerable and sick population.

Therapeutic Interventional (TI) trials are treatment studies that involve people who have a disease or underlying condition. They include the administration and testing of new treatments or new ways of using existing treatments, such as new drugs, vaccines, or cell therapies.

This Clinical Research Assistant is responsible for the overall management of clinical trials on the Myeloma Team.

• Working with the regulatory management team to complete all regulatory documentation in accordance with their role as required by the OHSU IRB and sponsor.
• Creation of study trackers and organization tools.
• Assisting in the verification of patient eligibility.
• Development of data collection instruments and assistance with regulatory.
• Data entry.
• Assurance of conduct of protocol in accordance with applicable NCI and FDA guidelines.
• Maintenance of study patient records and source documentation.
• Coordinating orders, scheduling and study drug administration with the clinical team.
• Supporting clinical care team with completion of research required tests and assessments.
• Act as liaison between research protocol and clinic staff, pharmacy, and research participants.
• Ensuring that patient billing is accurate and assisting manager and financial team in verifying appropriate clinical trial billing. Participation in patient consenting.
• Support and periodic coverage to and across study teams, as delegated by the Clinical Research Manager. This includes, but is not limited to: assisting with maintaining regulatory documents, patient visits and study assessments (e.g., ECGs, vitals, specimen collection, management and shipping, etc.), requesting medical records, and other study related tasks, as needed.

This TI Clinical Research Assistant will have direct patient contact, process biological samples, and may perform other non‑invasive testing such as ECGs. The TI Clinical Research Assistant will also assist in the continuing education of physicians, residents, interns, nurses and other related personnel with regards to knowledge of clinical trials and activities.

Education and experience:

• Bachelor's Degree in relevant field and 1 year of relevant experience OR
• Associate's and 3 years of relevant experience OR
• No degree and 4 years of relevant experience OR
• Equivalent combination of training and experience.

Required competencies:

• High degree of attention to detail
• Ability to prioritize and complete multiple tasks at one time
• Excellent communication, analytical, and organizational skills: both written and verbal
• Ability to work independently and as part of a team while being collaborative in resolving problems
• Proficiency with computers running Windows and PC applications (e.g., MS Excel, Oracle, Access, Word and PowerPoint)
• Demonstrated excellent customer service skills both on the phone and in person
• Possess energy and drive to coordinate multiple projects simultaneously
• Ability to use tact and diplomacy to maintain effective working relationships
• Critical thinking skills
• Time management skills

Every Knight Cancer employee is expected to embody our guiding principles:

• We act BOLDLY—Breakthroughs require pushing the boundaries of science, exploring new frontiers, and thinking differently.
• We SUPPORT each other—Respect leads to trust, which leads to excellence.
• We work as a CONNECTED team—We must leverage our collective brain power to conquer cancer because no one individual can do it alone.

• Clinical trial knowledge with a minimum of 1 year of research experience
• Oncology experience
• Experience conducting different phases of projects, including data collection and 3‑5 years of clinical trial experience
• Networking and database systems
• Medical terminology
  
  Working knowledge of Epic
• CCRP or ACRP Certification
• Typing 40+ wpm

Apply online. Please be sure to include a resume or CV and cover letter with your application.

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