The role involves independently coordinating and managing complex clinical research activities under the direction of a Principal Investigator
Job Summary
The role involves independently coordinating and managing complex clinical research activities under the direction of a Principal Investigator.
Candidates must ensure regulatory compliance, maintain data integrity, and efficiently execute study protocols while analyzing adverse events.
The position offers competitive benefits including up to 22 days of vacation, health insurance, and tuition coverage for employees and families.
Matching Summary
The role involves independently coordinating and managing complex clinical research activities under the direction of a Principal Investigator.
Salary
Base: $52,600.00 - $78,900.00 annually; Bonus/Equity: Not specified; Benefits: Up to 22 days vacation, health insurance, 403(b) retirement plan, tuition coverage
Skills & Requirements
Must-have
Coordinate complex clinical research activities
Ensure regulatory compliance with agencies
Analyze and report adverse events
Manage study protocols and amendments
Prepare manuscripts and grant proposals
Nice-to-have
Phlebotomy training or willingness to complete
Experience with statistical analysis software SAS
Database management skills
Spreadsheet analysis capabilities
Collaboration in scientific literature review
Key Requirements
Bachelor's degree or equivalent experience
2 years of Clinical Research work experience
Basic Life Support certification (with skills assessment)
Willingness to obtain BLS within one month of hire