Medical University of South Carolina
Healthcare
ResearchAssistant
“Research Assistant at Medical University of South Carolina. Skills: Clinical research, Data management, Regulatory compliance. Collect biological specimens. Process biological specimens”
Industry & Context.
Query resolution
Work on campus, Hybrid work after probation, Weekend work, After-hours work, Physical demands
What They're Looking For.
Must Have
High school diploma, Four years of relevant program experience, Bachelor's degree may substitute for program experience
What You'll Do.
Collect biological specimens
Process biological specimens
Ship biological specimens
Maintain specimen inventory
Schedule study visits
Schedule study assessments
Maintain regulatory documents
Complete pre-screening phone calls
Review medical charts
Speak with subjects about studies
Monitor lab kit inventory
Monitor study supply inventory
Destroy expired lab kits
Call subjects for appointments
Obtain signatures from staff
Assist with medical history collection
Assist with adverse event collection
Review outside medical records
Assist with study worksheet creation
Assist with source document creation
Perform phone marketing
Maintain screening logs
Maintain screening data entry
Prepare study supplies
Prepare study equipment
Prepare study documents
Conduct minimal risk studies independently
Perform minimal risk assessments
Perform greater than minimal risk assessments
Collect data from participant
Collect data from electronic medical record
Prepare biological specimens
Process biological specimens
Ship biological specimens
Maintain biological specimen inventory
Conduct consent for minimal risk studies
Document consent for minimal risk studies
Conduct consent for greater than minimal risk studies
File regulatory documents
File regulatory reports
Create regulatory submissions
Create simple regulatory reports
Submit personnel amendments
Submit continuing review applications
Prepare for study monitoring visits
Prepare for study audit visits
Address monitoring findings
Resolve study queries
Collect adverse events
Prepare adverse events
Process adverse events
File external SAE reports
Complete case report forms
Enter data into EDC systems
Create simple databases
Create simple data collection forms
Create simple surveys
Create simple source documents
Schedule team meetings
Coordinate team meetings
Prepare meeting documents
Safeguard human subjects research
Adhere to conflict of interest management plans
Maintain study compliance
Maintain institutional requirements
Maintain other policies
Maintain Delegation of Authority Logs
Perform administrative duties
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