The role involves assisting investigators in developing research plans and managing all phases of study protocols to ensure regulatory compliance
Job Summary
The role involves assisting investigators in developing research plans and managing all phases of study protocols to ensure regulatory compliance.
Candidates will coordinate multiple research studies simultaneously, acting as a liaison with the school, sponsoring agencies, and study participants.
The position offers competitive benefits including up to 22 days of vacation, health insurance packages, and tuition coverage for employees and families.
Matching Summary
The role involves assisting investigators in developing research plans and managing all phases of study protocols to ensure regulatory compliance.
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
Clinical research experience
Protocol management and compliance
Adverse event reporting
Nice-to-have
Manuscript preparation skills
Grant proposal assistance
Statistical analysis software SAS
Key Requirements
Bachelor's degree or equivalent experience
2 years of clinical research work experience
Basic Life Support certification within one month of hire