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

📋 Description

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

• Prepare precise study status reports and ensure the upkeep of study documentation.

• Efficiently manage queries generated by sponsors.

• Assume responsibility for cost-effectiveness in study execution.

• Engage in the preparation and evaluation of study documentation and feasibility analyses for new proposals.

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

• Guarantee patient safety and adherence to ICON's protocols, procedures, and regulatory standards.

⛳️ Requirements

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

• Relevant experience in clinical trial monitoring.

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

• Familiarity with ICH-GCP guidelines.

• Proficiency in reviewing and assessing medical data.

• Strong written and verbal English communication skills.

• Good interpersonal skills to address inquiries promptly.

• Willingness to travel as necessary (approximately 60%).

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

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Comprehensive 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.