Not specified; competitive salary offered; range o...
Not specified
Minimum 6 years pharmaceutical or cro experience
Minimum 2 years site monitoring or rbm experience
Knowledge of 21 cfr part 11 and ich e6 gcp
ICON Clinical Research is seeking an RBM Site Monitoring Lead to oversee clinical trial operations, ensuring high-quality outcomes and compliance across studies. The ideal candidate will have significant experience in site monitoring and a collaborative approach to problem-solving
Job Summary
The role involves maintaining high quality, consistency, and compliance with Sponsor procedures across clinical studies while recommending process adjustments based on data-driven trends.
As a change agent and subject matter expert, the incumbent will support study teams and participate in internal and external audits and inspections.
ICON offers a competitive salary along with comprehensive benefits including health insurance, retirement planning, and a global Employee Assistance Programme.
Matching Summary
Match Score: 85
ICON Clinical Research is seeking an RBM Site Monitoring Lead to oversee clinical trial operations, ensuring high-quality outcomes and compliance across studies. The ideal candidate will have significant experience in site monitoring and a collaborative approach to problem-solving.
Salary
Not specified; Competitive salary offered; Range of additional benefits provided
Skills & Requirements
Must-have
Minimum 6 years pharmaceutical or CRO experience
Minimum 2 years Site Monitoring or RBM experience
Knowledge of 21 CFR Part 11 and ICH E6 GCP
Ability to travel up to 50% including international
Nice-to-have
Pragmatic approach to evolving processes
Strong influence without authority skills
Growth mindset focused on diversity and inclusion
Experience with internal and external audits
Key Requirements
6+ years in pharmaceutical or CRO industry
2+ years in Site Monitoring or Risk-Based Monitoring
Robust understanding of drug development processes
Knowledge of regulatory standards 21 CFR Part 11 and ICH E6