Not specified; competitive within country; range o...
Fully remote
3 years relevant clinical supply experience
Knowledge of ich/gcp regulatory guidelines
Proficiency with ms word and excel
This role involves managing and coordinating clinical supplies activities to support the successful execution of clinical trials across multiple therapeutic areas
Job Summary
This role involves managing and coordinating clinical supplies activities to support the successful execution of clinical trials across multiple therapeutic areas.
The position requires independent initiation of IP shipments, tracking orders through receipt at investigator sites, and communicating with distribution vendors for timely delivery.
ICON offers a competitive salary along with comprehensive benefits including health insurance, retirement planning, and a global employee assistance program focused on well-being.
Matching Summary
This role involves managing and coordinating clinical supplies activities to support the successful execution of clinical trials across multiple therapeutic areas.
Salary
Not specified; Competitive within country; Range of additional benefits offered
Skills & Requirements
Must-have
3 years relevant clinical supply experience
Knowledge of ICH/GCP regulatory guidelines
Proficiency with MS Word and Excel
Experience in biotechnology or pharmaceutical industry
Fundamental knowledge of clinical drug development process
Nice-to-have
High level of agility and adaptability
Excellent organizational skills
Strong problem-solving abilities
Effective collaboration and communication
Action-oriented mindset
Key Requirements
Bachelor's Degree required
Minimum 3 years of relevant experience
Knowledge of International Council of Harmonization (ICH) guidelines