Clinical Research Scientist II

Preferred Education and Experience:

• Master’s degree in life sciences, nursing, public health, pharmacy, or other health related disciplines
• Experience in oncology, primary care, psychiatry, or cardiopulmonary clinical trials; with a common clinical trial enterprise system, such as, Oncore; in site monitoring; and in clinical research, population health, or genomics.
• Community health worker background preferred.
• Experience in healthcare, academic, biobanking or research environment.
• Competence in data cleaning techniques, OpenSpecimen (or other biobanking platforms), Research Electronic Data Capture software (REDCap), e-clinical works, and Microsoft Office.

Responsibilities:

Clinical Research

• Help develop protocol development and translational roadmaps for commercially oriented faculty led projects
• Liaison with compliance and privacy officers
• Ensure research is conducted in compliance with IRB approved protocols
• Work with clinical staff and providers in consenting patients for research projects
• Work as a patient liaison and advocate in longitudinal studies, including follow-up

Data Curation

• Support faculty and staff in data collection, quality control and curation 
• Occasionally abstract or transcribe electronic medical record (EMR) data for research data warehouse under supervision of study investigators

Administrative

• Performs other duties as assigned, including travel, ordering, coordinating meetings for clinical trial committees and research project teams