Non-Exempt Temporary or Casual- General Internal Medicine

Typical Duties may include:
Assist PIs with research, coordination, administration, planning and implementation of study;
Coordinate and monitor data collection activities; mostly remote but sometimes in-person work will be needed, remote work will be allowed as possible
Anticipate and resolve problems;
Applicant will participate in all phases of research;
Work as part of a team of other researchers on the study
Target and meet specific study recruitment goals;
Prepare REDCAP electronic data forms;
Prepare reports regarding study progress for the study team;
Organize investigator team meetings;
Coordinate UMN and other site study activities;
Coordinate IRB communications
Interface with the CTSI team who is helping with ct.gov account;
Assist with administration of informed consent as schedule demands;
Assist with data entry as schedule demands;
Assist with preparation on presentation and publications of research findings; 
Promptly contact the PIs for potentially serious adverse events;
Ensure compliance with human subjects, HIPAA, participant consent, and study personnel training requirements and other regulations.