Not specified; not specified; competitive within c...
Fully remote
Advanced degree in life sciences or nursing
Extensive experience as a clinical research associate
Working knowledge of early phase oncology trials
The role involves monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards
Job Summary
The role involves monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards.
ICON plc offers a competitive salary along with various benefits including health insurance, retirement planning, and global employee assistance programs.
Candidates will partner with a global biopharmaceutical client focused on developing breakthrough innovative medicines to fight cancer.
Matching Summary
The role involves monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards.
Salary
Not specified; Not specified; Competitive within country with range of additional benefits
Skills & Requirements
Must-have
Advanced degree in life sciences or nursing
Extensive experience as a Clinical Research Associate
Working knowledge of early Phase Oncology trials
Strong understanding of GCP standards and regulatory requirements
Nice-to-have
Ability to influence and drive compliance
Experience managing multiple sites simultaneously
Excellent stakeholder management skills
Key Requirements
Advanced degree in relevant field such as life sciences, nursing, or medicine
Proven ability to manage multiple sites and projects simultaneously
Working knowledge in monitoring complex, early Phase Oncology trials