Bachelor's degree in life sciences or nursing certification
Valid driver's license where applicable
This role involves performing and coordinating all aspects of clinical monitoring and site management to ensure protocol compliance and data reliability
Job Summary
This role involves performing and coordinating all aspects of clinical monitoring and site management to ensure protocol compliance and data reliability.
Candidates will conduct remote or on-site visits using a risk-based monitoring approach to identify failures and implement corrective actions.
The position offers a comprehensive Total Rewards package including medical plans, paid time off, retirement savings, and stock purchase opportunities.
Matching Summary
This role involves performing and coordinating all aspects of clinical monitoring and site management to ensure protocol compliance and data reliability.
Salary
Base: $100,000.00–$112,938.00; Bonus/Equity: Variable annual bonus based on performance; Benefits: Comprehensive medical, dental, vision, 401(k), PTO, and parental leave
Skills & Requirements
Must-have
1-3 years onsite pharmaceutical CRA experience
Bachelor's degree in life sciences or nursing certification
Valid driver's license where applicable
Knowledge of ICH-GCP guidelines and regulations
Risk-based monitoring concepts and processes
Nice-to-have
Experience with oncology, HIV, respiratory, or vaccine trials
Strong critical thinking and root cause analysis skills
Excellent oral and written communication abilities
Ability to work independently and in a team environment
Flexibility to adapt to various scenarios
Key Requirements
Must be legally authorized to work in the United States without sponsorship
Pass a comprehensive background check including drug screening
CRA Level II experience equivalent to 1+ years as a clinical research monitor
Bachelor's degree in life sciences or Registered Nursing certification
Work Rights
Must be legally authorized to work in the United States without sponsorship