Clinical Research Associate

Icon Clinical Plc; Varese; In loco; EUR 42.000 - 64.000; Tempo pieno

Vantaggi offerti da questo lavoro

Health coverage

Dental coverage

Vision coverage

Retirement plans

Life assurance

Disability coverage

Employee assistance program

Wellbeing resources

Structured training

Descrizione del lavoro

ICON Clinical Plc in Lombardia, Italy is seeking a CRA II to design and analyze clinical trials, monitor sites, collaborate with investigators, and contribute to study documentation. You will help uphold data integrity and patient safety while advancing innovative therapies.

The role supports cross-functional teams in a fast-paced, global environment, requires travel (about 60%), and offers learning and development opportunities along with competitive incentives.

Competenze

• Bachelor's degree in 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.
• Strong organizational and communication skills with attention to detail.
• Willingness to travel approximately 60%.

Mansioni

• Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
• Ensure protocol compliance, data integrity, and patient safety throughout the trial process
• Collaborate with investigators and site staff to facilitate smooth study conduct
• Perform data review and resolution of queries to maintain high-quality clinical data
• Contribute to preparation and review of study documentation, including protocols and clinical study reports

Conoscenze

Site monitoring

Data review

Regulatory compliance

ICH-GCP guidelines

Study documentation

Communication skills

Independent worker

Formazione

Bachelor's degree in scientific or healthcare-related field

Descrizione del lavoro

As a CRA II at ICON, you design and analyze clinical trials, ensuring data integrity and patient safety while advancing innovative therapies. You will monitor sites, collaborate with investigators, and contribute to study documentation. This role supports cross-functional teams in a fast-paced, global environment and involves travel. You will help bring new medicines to patients faster by upholding high-quality standards and regulatory compliance.

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways
• Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
• Ensure protocol compliance, data integrity, and patient safety throughout the trial process
• Collaborate with investigators and site staff to facilitate smooth study conduct
• Perform data review and resolution of queries to maintain high-quality clinical data
• Contribute to preparation and review of study documentation, including protocols and clinical study reports
• Bachelor's degree in 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
• Strong organizational and communication skills with attention to detail
• Ability to work independently and collaboratively in a fast-paced environment
• Willingness to travel as required (approximately 60%)
• Strong communication
• Knowledge of clinical trial processes and ICH-GCP
• Data review and query resolution
• Regulatory compliance understanding

Clinical Research Associate varese, lombardia, it