Assist the management of research study daily operations, monitoring protocol compliance and patient toxicities, adverse event reporting and regulatory submissions (IRB, FDA). May act as a project manager for specific protocols. Independently interact with study sponsors and provide all necessary documentation in a timely manner. Mentor junior staff on research protocols and provide support.

Assist senior staff with database build and management, monitoring and issuing queries, performing analyses as needed, running reports, and presenting information to relevant stakeholders

Support new clinical trial start-up procedures though development of necessary regulatory documents to align with OHSU’s required template and language, develop visit schedule in OHSU’s CTMS, and provide additional support as needed.

Complete special projects under the guidance of one of the group epidemiologists, including manuscript review, database support, etc.