TI Sr Clinical Research Assistant (Clinical Research Coordinator)
On-sitePortland, Oregon, United States
Portland, Oregon, United StatesOn-siteContractSenior LevelLarge
ContractSenior LevelLarge
Job Summary
Coordinate orders, schedule study drug administration, and verify patient eligibility for therapeutic interventional oncology trials. Assist the regulatory team with documentation, create study trackers, and ensure protocol compliance with NCI and FDA guidelines. Manage patient records, source documentation, and billing verification while acting as a liaison between the clinic, pharmacy, and participants. Support the clinical care team with research assessments, biological sample processing, and periodic coverage across study teams. Participate in patient consenting and assist in continuing education for medical staff.
Required Qualifications
- Bachelor's Degree in relevant field
- 1 year of relevant experience
- Associate's degree and 3 years of relevant experience
- No degree and 4 years of relevant experience
- Equivalent combination of training and experience
- 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
Desired Qualifications
- Clinical trial knowledge with a minimum of 1 year of research experience
- Oncology experience
- Experience conducting different phases of projects, including data collection
- 3-5 years of clinical trial experience
- Networking and database systems
- Medical terminology
- Working knowledge of Epic
- CCRP or ACRP Certification
- Typing 40+ wpm
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