Competitive salary; benefits include annual leave,...
Fully remote
Extensive experience as clinical research associate
Strong understanding of clinical trial processes
Expertise in good clinical practice standards
The role involves leading clinical trial monitoring tasks with a focus on quality and continuous improvement while ensuring adherence to protocols and regulatory requirements
Job Summary
The role involves leading clinical trial monitoring tasks with a focus on quality and continuous improvement while ensuring adherence to protocols and regulatory requirements.
ICON offers a competitive salary along with benefits including health insurance, retirement planning, and a global Employee Assistance Programme for well-being support.
Candidates must have a Bachelor's degree in a scientific or healthcare field and extensive experience managing multiple sites simultaneously.
Matching Summary
The role involves leading clinical trial monitoring tasks with a focus on quality and continuous improvement while ensuring adherence to protocols and regulatory requirements.
Salary
Competitive salary; Benefits include annual leave, health insurance, retirement planning, and life assurance; Flexible country-specific optional benefits available
Skills & Requirements
Must-have
Extensive experience as Clinical Research Associate
Strong understanding of clinical trial processes
Expertise in Good Clinical Practice standards
Proficiency in relevant clinical trial software
Willingness to travel approximately 60%
Nice-to-have
Ability to influence and drive compliance
Strong organizational and problem-solving skills
Experience guiding others independently
Excellent stakeholder management skills
Key Requirements
Bachelor's degree in relevant scientific discipline