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

📋 Description

• Executing clinical trial monitoring tasks to a high standard.

• Collaborating closely with your team and relevant stakeholders.

• Overseeing all activities involved in setting up and monitoring a study.

• Preparing precise study status reports and managing study documentation.

• Effectively addressing sponsor-generated queries.

• Contributing to the preparation and evaluation of study documentation and feasibility studies for new proposals as needed.

• Building and nurturing strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.

• Safeguarding patient safety by ensuring adherence to ICON's procedures, protocols, and regulatory standards.

⛳️ Requirements

• Bachelor's degree in medicine, science, or a related field.

• Understanding of ICH-GCP guidelines and the ability to review and assess medical data.

• Exceptional written and verbal communication skills in English.

• Strong interpersonal skills, allowing you to handle queries promptly.

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

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

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

• Retirement and pension schemes.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

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