Clinical Research Associate II – Monitoring & Data

KCR Placement; Chicago (IL); Sur place; USD 70 000 - 95 000; Plein temps

Avantages offerts par ce poste

Annual leave

Health insurance

Retirement planning

Employee assistance program (LifeWorks

Life assurance

Flexible benefits

Résumé du poste

ICON is seeking a Clinical Research Associate to support site qualification, initiation, monitoring, and close-out visits in Chicago. You will ensure protocol adherence, data integrity, and patient safety while collaborating with investigators and study staff.

The role requires a Bachelor's in a science/healthcare field, 2+ years of CRA experience, strong organizational and communication skills, and travel about 60%. ICON offers a competitive salary and comprehensive benefits.

Qualifications

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Strong organizational and communication skills, with attention to detail.
• Ability to work independently and collaboratively in a fast-paced environment.
• Willingness to travel as required (approximately 60%).

Responsabilités

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Connaissances

CRA experience

ICH-GCP knowledge

Organizational skills

Communication skills

Travel ability

Independent & collaborative work

Formation

Bachelor's degree in science/healthcare

Description du poste

ICON is seeking a Clinical Research Associate to support site qualification, initiation, monitoring, and close-out visits in Chicago. You will ensure protocol adherence, data integrity, and patient safety while collaborating with investigators and study staff.

The role requires a Bachelor's in a science/healthcare field, 2+ years of CRA experience, strong organizational and communication skills, and travel about 60%. ICON offers a competitive salary and comprehensive benefits.