Senior Clinical Research Associate

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

📋 Description

• Conduct site qualification, initiation, 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 the smooth execution of studies.

• Perform data reviews and resolve queries to uphold high-quality clinical data.

• Assist in the preparation and review of study documentation, including protocols and clinical study reports.

• Take charge of clinical trial monitoring deliverables and work in a collaborative manner.

⛳️ 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 skills, with a keen attention to detail.

• Capability to work both independently and as part of a team in a dynamic environment.

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

• Proficiency in both German and English languages.

• Employment with ICON is subject to possessing the legal right to work in the country where the position is based.

🏝️ Benefits

• Competitive base salary and performance-related incentives.

• Health and wellbeing programs that include medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life assurance and disability coverage.

• Employee assistance programs and wellbeing resources.

• Opportunities for learning and development through structured training and career pathways.