Clinical Research Associate 1

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

📋 Description

• Provide high-quality clinical trial monitoring services.

• Oversee all tasks related to the setup and monitoring of a study.

• Prepare precise study status reports and manage study documentation.

• Efficiently handle sponsor-generated queries.

• Take charge of ensuring cost efficiency for the study.

• Engage in the preparation and evaluation of study documentation and feasibility assessments for new proposals.

• Build and sustain cooperative relationships with key stakeholders, clinical investigators, and site personnel.

• Safeguard patient safety while adhering to ICON procedures, protocols, and regulatory standards.

⛳️ Requirements

• A university degree in medicine, science, or a related field.

• Relevant experience in clinical trial monitoring.

• Familiarity with ICH-GCP guidelines.

• Ability to review and assess medical data effectively.

• Outstanding written and verbal communication skills in English.

• Strong interpersonal skills to manage queries promptly.

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

• Legal authorization to work in Belgium.

🏝️ Benefits

• Competitive base salary along with performance-based incentives.

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

• Reasonable accommodations provided during the recruitment process.