Clinical Research Associate

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

📋 Description

• Executing clinical trial monitoring tasks to an exceptional standard

• Operating independently while coordinating all activities necessary for the setup and oversight of a study

• Producing precise study status reports and upholding study documentation

• Efficiently managing sponsor-generated inquiries and ensuring the cost-effectiveness of the study

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

• Building and nurturing 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

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

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

• Outstanding written and verbal communication skills in English

• Strong interpersonal skills that allow you to address inquiries promptly

• Readiness to travel as needed (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 pathways