Clinical Research Associate 1

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

📋 Description

• Providing high-quality clinical trial monitoring services.

• Taking initiative to independently coordinate all aspects of study setup and monitoring.

• Accurately completing study status reports and maintaining necessary documentation.

• Efficiently addressing sponsor-generated queries while ensuring cost-effectiveness in the study.

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

• Building and sustaining strong, collaborative relationships with key stakeholders, clinical investigators, and site personnel.

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

⛳️ Requirements

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

• Familiarity with ICH-GCP guidelines and the ability to assess and interpret medical data.

• Exceptional written and verbal communication skills in English.

• Strong interpersonal skills to address 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 plans.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

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