Coordinates data collection and adverse event reporting
The role involves assisting investigators as a coordinator for complex medical oncology clinical research studies while acting as a liaison between the school, sponsors, and participants
Job Summary
The role involves assisting investigators as a coordinator for complex medical oncology clinical research studies while acting as a liaison between the school, sponsors, and participants.
Candidates will be responsible for managing all phases of study protocols, ensuring compliance with regulatory agencies, and analyzing collected clinical data to report progress trends.
The position offers competitive benefits including up to 22 days of vacation, health insurance packages, and tuition coverage for employees and their families.
Matching Summary
The role involves assisting investigators as a coordinator for complex medical oncology clinical research studies while acting as a liaison between the school, sponsors, and participants.
Salary
Base: $52,600.00 - $78,900.00 annually; Bonus/Equity: Not specified; Benefits: Up to 22 days vacation, health insurance, retirement plan, tuition coverage
Skills & Requirements
Must-have
manages complex clinical research studies
ensures regulatory compliance with protocols
coordinates data collection and adverse event reporting
Nice-to-have
experience preparing grant proposals
collaboration in manuscript preparation
knowledge of statistical analysis software SAS
Key Requirements
Bachelor's degree or equivalent experience
2 years of clinical research work experience
Basic Life Support certification (with skills assessment)