Research Data Analyst I - Military veterans preferred

Oregon Health & Science University

Oregon Health & Science University values a diverse and culturally competent workforce. We are proud of our commitment to being an equal opportunity, affirmative action organization that does not discriminate against applicants on the basis of any protected class status, including disability status and protected veteran status. Individuals with diverse backgrounds and those who promote diversity and a culture of inclusion are encouraged to apply. To request reasonable accommodation contact the Affirmative Action and Equal Opportunity Department at 503-494-5148 or aaeo@ohsu.edu.


Research Data Analyst I

US-OR-Portland

Job ID: 2025-34050
Type: Regular Full-Time
# of Openings: 1
Category: Research
Portland, OR (Downtown)

Overview

• Supporting data management of both FDA-regulated and non-FDA-regulated clinical trial protocols and research projects, both within IDRU and across OHSU collaborators. These tasks include helping with the development of statistical analysis plans, database build and management, running data validations and querying data, interface with study Sponsors, help to manage IRB submissions and approvals, provide reports for IND submissions to the FDA, and data analyses and interpretation. 

• Participate in the IDRU’s Data Team work, including supporting study design, conducting data analyses, utilizing appropriate statistical methods, providing education, training, and to colleagues within the team, and communicate with stakeholders as needed. 

• Help manage study coordination work for several NTM-focused clinical trials, or research protocols, with a focus on data-specific tasks. Responsibilities may include unblinded staff tasks, such as monitoring data, preparing DMC reports, meeting with DMSB and communicating results with sites, interfacing with study Sponsor, and managing regulatory documentation. 

• Support new clinical trial start-up procedures by providing necessary regulatory documents to align with OHSU’s required template and language, develop visit schedule in OHSU’s CTMS, review study feasibility, and provide additional support as needed. 

• Master’s Degree in relevant field OR

• Bachelor’s Degree in relevant field AND 2 years of relevant experience

• Strong written, verbal comminication and proficeincy in MS Office Suite; meticulous record keeping and organization skills.

• Working knowledge of IRB guidelines and FDA, DHHS, other agency guidelines that govern clinical research.

• STATA, SAS, R, SPSS, or other statistical software.

• MPH in Epidemiology or Biostatistics, or currently working toward MPH in Epidemiology or Biostatistics
• 2-3 years of experience in clinical research including at least 2 years of data analyses, database management, and communicating with stakeholders.
• REDCap database management.
• Experience with EndNote or other citation software.
• Good Clinical Practice (GCP) Certification, SOCRA or ACRP Certification
• Phlebotomy training

PI269724581