Clinical Research Associate

This is a fully remote position, open to applicants in Italy.

📋 Description

• Conduct site qualifications, initiations, monitoring, and close-out visits for clinical trials.

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

• Collaborate with investigators and site personnel to ensure seamless study execution.

• Perform data reviews and resolve queries to uphold the quality of clinical data.

• Assist in the preparation and assessment of study documents, including protocols and clinical study reports.

• Assume responsibility for clinical trial monitoring deliverables and work cooperatively in a sponsor-dedicated model.

⛳️ Requirements

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

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

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

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

• Capability to work independently as well as in a team-oriented environment in a fast-paced setting.

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

• Legal authorization to work in Italy.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellness programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Learning and development opportunities through structured training and career pathways.