Clinical Research Associate
Clinical Research Associate At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.
As the world’s largest FSP organisation, with over 90 sponsor partnerships,
we offer
stability, career development and a collaborative environment where your work contributes to the development of treatments that agevolazioni patients worldwide.
As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
What You Will Do:You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
Performing data review and resolution of queries to maintain high-quality clinical data.
Contributing to the preparation and review of study documentation,
including protocols and clinical study reportsYour Profile:You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Required qualifications and
experience:
Bachelor's degree in a scientific or healthcare-related field.
Minimum of 2 years of experience as a Clinical Research Associate.
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
Rewards & BenefitsICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:Competitive base salary and performance related incentivesHealth and wellbeing programmes including medical, dental, and vision coverage where applicableRetirement and pension plansLife assurance and disability coverageEmployee assistance programmes and wellbeing resourcesLearning and development opportunities through structured training and career pathwaysBenefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Italy, MilanType: Full time
As the world’s largest FSP organisation, with over 90 sponsor partnerships,
we offer
stability, career development and a collaborative environment where your work contributes to the development of treatments that agevolazioni patients worldwide.
As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
What You Will Do:You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
Performing data review and resolution of queries to maintain high-quality clinical data.
Contributing to the preparation and review of study documentation,
including protocols and clinical study reportsYour Profile:You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Required qualifications and
experience:
Bachelor's degree in a scientific or healthcare-related field.
Minimum of 2 years of experience as a Clinical Research Associate.
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
Rewards & BenefitsICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:Competitive base salary and performance related incentivesHealth and wellbeing programmes including medical, dental, and vision coverage where applicableRetirement and pension plansLife assurance and disability coverageEmployee assistance programmes and wellbeing resourcesLearning and development opportunities through structured training and career pathwaysBenefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Italy, MilanType: Full time