TI Clinical Research Assistant at Oregon Health & Science University

Portland, Oregon, United States -

Full Time

Start Date

Immediate

Expiry Date

18 Aug, 26

Salary

77521.6

Posted On

20 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research Coordination, Patient Scheduling, Data Collection, Good Clinical Practice, HIPAA Compliance, IRB Reporting, Patient Assessment, Patient Consent, Phlebotomy, Vital Signs Assessment, Microsoft Office Suite, Electronic Data Entry, Regulatory Documentation, Budget Negotiation, Quality Assurance Audits, Customer Service

Industry

Higher Education

Description

Department Overview Under general supervision, assists in coordinating the details of therapeutic interventional research studies and protocol documentations, patient scheduling, and data collection. Assists in complex studies. Works under the direction of a Principal Investigator or other Project Coordinators or Project Managers. Will provide assistance to coordinate and conduct multiple research protocols in a team setting. This will involve working closely with multiple OHSU clinical and research areas, including the research pharmacy, the Epic team, and the clinical research billing office. Will interface and work with industry sponsors to ensure proper and compliant study conduct. Works closely with research and clinical investigators and team members across multiple sites to ensure the safety of research participants. Is able to set priorities and timelines for complex research activities. Exercises judgment within defined Good Clinical Practice and HIPAA guidelines to determine appropriate action via reporting mechanisms and structures (Institutional Review Board) in recognizing adverse events, protocol deviations, and other unanticipated study problems and reports to senior staff appropriately. May assist with project logistics and all parts of research program coordination or management, in coordination with other OHSU clinical and research departments. May collate, enter, and present research data for analysis. May assist with administrative and regulatory duties related to the study as assigned. Additional duties as assigned. Must have excellent communication, organization, and customer service skills, and must be a self-starter with ability to work well in a team environment. Familiarity with health record database systems is helpful. Responsible for patient assessment for protocol eligibility, counseling of patients regarding study schemas; study calendar and treatment plan; thorough written tracking of patient visits’ for billing purposes, patient education; coordinating follow-up care and liaison between patients and other members of the healthcare research team. Will be responsible for the coordination of multiple research studies for the Nephrology Research team including maintenance and submission of patient data; evaluation of protocol activities; maintenance and preparation of quality assurance audits, and management of investigational drugs. Ensures timely completion of work for all assigned trials. Function/Duties of Position Coordinate with OPAM and Contracts office during budget and contract negotiation process Coordinates with DoM office and OPAM for account maintenance, invoicing, and reconciliation. Actively screen and consent patients for the studies and conduct study visits. This will include coordinating appointments with the PI and/or sub-PI as needed. Submit modification approvals to the IRB and complete all other IRB reportorial requirements Complete electronic data entry for research patients in a timely manner. Maintain and organize study binders, as well as prepare for site visits and meet with monitors. Participate in recruitment activities for active studies. Coordinate care of research patients with their specialists/PCPs Required Qualifications Bachelor's in relevant field OR Associate's AND2 years of relevant experience OR3 years of relevant experience OR Equivalent combination of training and experience Preferred Qualifications Bachelor’s degree with major courses in the field of research is preferred. Prior research experience in a university setting. Basic clinical examination & vital signs assessment is preferred. Knowledge of phlebotomy also preferred. Familiarity with health record and research database systems. Must have excellent communication, organization, and customer service skills, and must be a self-starter Proficient knowledge of Microsoft Office Suite (including Word, Outlook, and Excel); strong organizational skills; excellent oral and written communication skills; meticulous detail to data and study procedures; ability to prioritize work demands and trouble shoot; ability to work independently in a multi-task environment. Familiarity with health record database systems is helpful. Additional Details General work schedule will be a flexible Monday – Friday shifts (5 days per week). Environmental exposures include working with lab reagents, human tissues (blood and saliva), and general patient contact. Ability to work at a computer for up to four hours at a time. Ability to move around the campus as needed for research studies and meetings. Ability to lift up to 25 pounds. Why apply to OHSU? We are Oregon's only public academic health center. In addition to caring for patients, we lead groundbreaking research. We also train the next generation of health care professionals. As Portland's largest employer, we give you opportunities to learn and advance in a system of hospitals and clinics across Oregon and Southwest Washington. All are welcome. OHSU welcomes people of all ages, ethnicities, genders, national origins, religions and sexual orientations. We are striving to build an anti-racist, multicultural institution and encourage people with diverse backgrounds to apply. To request reasonable accommodation, contact askhr@ohsu.edu

Responsibilities

Coordinates therapeutic interventional research studies, including patient screening, consenting, and data collection for the Nephrology Research team. Manages protocol documentation, IRB submissions, and interfaces with industry sponsors and clinical investigators to ensure compliant study conduct.