Clinical Research Associate

This is a fully remote position, open to applicants in Kansas, +3 more states.

📋 Description

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

• Prepare precise reports on study status and manage study-related documentation.

• Efficiently address sponsor-generated queries and ensure the study operates within budgetary constraints.

• Engage in the development and review of study documentation and feasibility assessments for new proposals as needed.

• Foster and sustain cooperative relationships with essential stakeholders, clinical investigators, and site personnel.

• Safeguard patient well-being and ensure adherence to ICON procedures, protocols, and regulatory standards.

⛳️ Requirements

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

• Relevant experience in clinical trial monitoring.

• Experience in monitoring Ophthalmology trials or multi-therapeutic areas.

• Familiarity with ICH-GCP guidelines.

• Ability to review and assess medical data effectively.

• Strong written and verbal communication skills in English.

• Good interpersonal skills to handle queries promptly.

• Willingness to travel as necessary, approximately 60% of the time.

• Legal authorization to work in the country where the position is located.

🏝️ Benefits

• 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 advancement pathways.