Clinical Research Associate

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

📋 Description

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

• Prepare precise study status reports and maintain thorough study documentation

• Efficiently manage sponsor-generated inquiries and take charge of study cost-effectiveness

• Contribute to the creation and assessment of study documentation and feasibility studies for new proposals as necessary

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

• Ensure the safety of patients and adherence to ICON's procedures, protocols, and regulatory standards

• Provide high-quality clinical trial monitoring across various clinical programs

⛳️ Requirements

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

• Exceptional written and verbal communication skills in both English and German

• Laboratory experience and/or capability to analyze laboratory results

• Background or interest in medical devices

• Strong interpersonal skills to address inquiries promptly

• Readiness to travel as needed (approximately 60%)

• Employment with ICON is contingent upon possessing the legal right to work in the country where the position is located

🏝️ Benefits

• Stability, opportunities for career advancement, and a collaborative workplace

• 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

• Reasonable accommodations provided during the recruitment process