Senior Clinical Research Associate

This is a fully remote position, open to applicants in Connecticut, +1 more state.

📋 Description

• Oversee all activities related to the setup and monitoring of a study.

• Prepare precise study status reports and manage study documentation.

• Efficiently handle sponsor-generated queries.

• Ensure cost efficiency throughout the study.

• Engage in the preparation and assessment of study documentation and feasibility studies for new proposals as needed.

• Foster and maintain collaborative relationships with key stakeholders, clinical investigators, and site personnel.

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

⛳️ Requirements

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

• Relevant experience in clinical trial monitoring.

• Familiarity with ICH-GCP guidelines.

• Ability to review and assess medical data effectively.

• Exceptional written and verbal communication skills in English.

• Strong interpersonal skills to address queries promptly.

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

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

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

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

• Retirement and pension plans.

• Life assurance and disability coverage.

• Employee assistance programs and wellbeing resources.

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