Clinical Research Associate

This is a fully remote position, open to applicants in Nebraska, +2 more states.

📋 Description

• Execute clinical trial monitoring tasks to an exemplary standard

• Oversee all aspects of study setup and monitoring activities

• Produce precise study status updates and keep study documentation organized

• Address sponsor-generated inquiries efficiently and manage study cost-effectiveness

• Contribute to the creation and evaluation of study documentation and feasibility assessments for new proposals as necessary

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

• Prioritize patient safety while ensuring adherence to ICON's procedures, protocols, and regulatory standards

⛳️ Requirements

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

• Familiarity with ICH-GCP guidelines

• Ability to review and assess medical data effectively

• Strong written and verbal communication skills in English

• Excellent interpersonal skills for addressing inquiries promptly

• Willingness to travel as necessary (approximately 60%)

• Employment subject to possessing the legal right to work in the location of the role

• Experience in monitoring Ophthalmology trials or multi-therapeutic areas

• Relevant experience in clinical trial monitoring

🏝️ Benefits

• Competitive base salary along with performance-related incentives

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

• Retirement and pension schemes

• Life insurance and disability coverage

• Employee assistance programs and wellbeing resources

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