Clinical Research Associate — Central/Midwest Monitoring

ICON Strategic Solutions; Illinois; On-site; USD 91,000 - 114,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

Employee assistance program

Life insurance

Flexible country-specific benefits

Job summary

ICON Strategic Solutions seeks a Clinical Research Associate to support central/Mid-West monitoring in a sponsor-dedicated model. You will contribute to high-quality clinical trial operations and collaborate with teams to deliver data-driven outcomes across programmes.

Requirements include a university degree in medicine or science, strong knowledge of ICH-GCP, excellent English communication, and willingness to travel up to 60%.

Qualifications

• University degree in medicine, science, or equivalent.
• Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data.
• Excellent written and verbal communication in English.
• Good social skills enabling you to deal with queries in a timely manner.
• Willingness to travel as required (approximately 60%).

Responsibilities

• Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation.
• Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.
• Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
• Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements.

Skills

ICH-GCP knowledge

English communication

Social skills

Willingness to travel 60%

Education

University degree in medicine, science, or equivalent

Job description

ICON Strategic Solutions seeks a Clinical Research Associate to support central/Mid-West monitoring in a sponsor-dedicated model. You will contribute to high-quality clinical trial operations and collaborate with teams to deliver data-driven outcomes across programmes.

Requirements include a university degree in medicine or science, strong knowledge of ICH-GCP, excellent English communication, and willingness to travel up to 60%.