
TI Sr. Clinical Research Assistant (Clinical Research Coordinator)
Oregon Health & Science University
- Portland, OR
- $50,128 per year
- Permanent
- Full-time
- 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.
- 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
- 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
- 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