Not specified; not specified; competitive salary w...
Extensive experience as a clinical research associate
In-depth knowledge of ich-gcp guidelines
Proven track record managing complex clinical trials
The role involves leading site management activities including selection, initiation, monitoring, and close-out visits to ensure regulatory compliance
Job Summary
The role involves leading site management activities including selection, initiation, monitoring, and close-out visits to ensure regulatory compliance.
Candidates will serve as the primary point of contact for clinical sites while mentoring CRAs to drive team performance and data integrity.
ICON offers competitive benefits including health insurance, retirement planning, and a global Employee Assistance Programme focused on well-being.
Matching Summary
The role involves leading site management activities including selection, initiation, monitoring, and close-out visits to ensure regulatory compliance.
Salary
Not specified; Not specified; Competitive salary with range of additional benefits
Skills & Requirements
Must-have
Extensive experience as a Clinical Research Associate
In-depth knowledge of ICH-GCP guidelines
Proven track record managing complex clinical trials
Strong leadership and mentoring skills
Nice-to-have
Advanced degree in life sciences or related field
Ability to foster an inclusive environment
Proactive approach to managing site performance
Key Requirements
Bachelor's degree in life sciences, nursing, pharmacy, or related field
Extensive experience within pharmaceutical, biotech, or CRO industry
Knowledge of regulatory requirements and clinical trial processes