TI Sr Clinical Research Assistant
About The Position
The Oregon Stroke Center Clinical Research Coordinator is responsible for initiation and maintenance of complex therapeutic interventional clinical research focused in vascular neurology. This position may assist with other studies for different neurological subspecialties. This includes: Acute stroke call coverage for after-hours study enrollments including Assisting on-call doctor with identifying inclusion and exclusion criteria Randomizing study patient Coming to the hospital to collect specimens and ensure study protocol is met Troubleshooting any issues that may come up Study initiation including Create study binders using protocol given by the sponsor Ensure study specific orders are available in Epic Collaborate with the Research Project Manager and Division Manager Order necessary labs and equipment from sponsor Arrange site initiation visit with sponsor Train all other study coordinators and research assistants on protocol Recruitment activities Study assessments and patient visits CRF documentation and data entry Maintain certificates as specified by each sponsor Coordinating care for patients enrolled in multiple clinical research protocols Collaborates with various OHSU departments to complete protocol required tests and procedures. This includes Interventional Radiology, Radiology, Research Pharmacy, Epic Informatics Team and other areas. Monitoring study compliance relating to the human subjects committee, the federal government and study sponsors Directly working with sponsors and monitors to ensure compliance with study protocols and reviewing deviations Active management of expectations and timelines of multiple studies Ensure quality assurance and participant safety Communicate effectively with other Clinical Research Coordinators and Assistants to delegate tasks as needed in a timely manner Processing and shipping study specimens This position works closely with other Clinical Research Coordinators, Clinical Research Assistants and Neurologists to fulfill the needs of the various research studies. Every coordinator is required to understand each study to help cover for absences and to enroll when on call.
Requirements
- Bachelor’s degree in relevant field AND 1 year of relevant experience, OR Associate’s degree AND 3 years of relevant experience, OR 4 years of relevant experience, OR Equivalent combination of training and experience
- Clinical research experience
- Strong interpersonal skills
- Commitment to working in a team environment
- Excellent written and verbal skills
- Highly organized and able to work independently
- Strong attention to detail
- Problem solving skills
- Able to perform the essential functions of the position with or without accommodation
- Ability to be flexible and adaptable to changes in the day-to-day workflow
Responsibilities
- Acute stroke call coverage for after-hours study enrollments including Assisting on-call doctor with identifying inclusion and exclusion criteria
- Randomizing study patient
- Coming to the hospital to collect specimens and ensure study protocol is met
- Troubleshooting any issues that may come up
- Study initiation including Create study binders using protocol given by the sponsor
- Ensure study specific orders are available in Epic
- Collaborate with the Research Project Manager and Division Manager
- Order necessary labs and equipment from sponsor
- Arrange site initiation visit with sponsor
- Train all other study coordinators and research assistants on protocol
- Recruitment activities
- Study assessments and patient visits
- CRF documentation and data entry
- Maintain certificates as specified by each sponsor
- Coordinating care for patients enrolled in multiple clinical research protocols
- Collaborates with various OHSU departments to complete protocol required tests and procedures. This includes Interventional Radiology, Radiology, Research Pharmacy, Epic Informatics Team and other areas.
- Monitoring study compliance relating to the human subjects committee, the federal government and study sponsors
- Directly working with sponsors and monitors to ensure compliance with study protocols and reviewing deviations
- Active management of expectations and timelines of multiple studies
- Ensure quality assurance and participant safety
- Communicate effectively with other Clinical Research Coordinators and Assistants to delegate tasks as needed in a timely manner
- Processing and shipping study specimens
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
5,001-10,000 employees
