The role involves overseeing complex multi-site clinical research studies within the field of medical oncology
Job Summary
The role involves overseeing complex multi-site clinical research studies within the field of medical oncology.
Candidates must ensure strict compliance with regulatory agencies and manage all phases of study protocols.
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 overseeing complex multi-site clinical research studies within the field of medical oncology.
Salary
Base: $62,000.00 - $96,100.00 annually; Bonus/Equity: Not specified; Benefits: Up to 22 days vacation, health insurance, 403(b) retirement plan, tuition coverage
Skills & Requirements
Must-have
3 years clinical research experience
protocol development and management
adverse event documentation
IRB protocol management issues
data collection and coding
Nice-to-have
manuscript preparation skills
grant proposal collaboration
statistical analysis software SAS
database management expertise
team supervision and training
Key Requirements
Bachelor's degree or equivalent experience
Basic Life Support certification (with skills assessment)