Clinical Research Associate

📋 Description

• You will play a key role in monitoring clinical trials, taking ownership of your responsibilities and working in a collaborative manner.

• Responsible for conducting site qualifications, initiating, monitoring, and closing out visits for clinical trials.

• Ensure compliance with protocols, maintain data integrity, and prioritize patient safety throughout the trial process.

• Work together with investigators and site personnel to ensure the smooth execution of studies.

• Engage in data review and resolve queries to uphold high standards of clinical data quality.

• Assist in the creation and evaluation of study documentation, including protocols and clinical study reports.

⛳️ Requirements

• A Bachelor's degree in a scientific or healthcare-related discipline.

• At least 2 years of experience as a Clinical Research Associate following certification.

• Comprehensive understanding of clinical trial processes, relevant regulations, and ICH-GCP guidelines.

• Excellent organizational and communication skills, with a keen eye for detail.

• Capability to work autonomously as well as part of a team in a dynamic environment.

• Willingness to travel as needed (approximately 60%).

• Certification in accordance with Italian Legislation.

🏝️ Benefits

• Various annual leave entitlements.

• A selection of health insurance options tailored to meet the needs of you and your family.

• Competitive retirement planning solutions to optimize savings and ensure confident planning for the future.

• Global Employee Assistance Programme, TELUS Health, providing 24-hour access to a worldwide network of over 80,000 independent specialized professionals dedicated to supporting your and your family’s well-being.

• Life assurance.

• Flexible country-specific optional benefits, such as childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.