Clinical Trial Monitoring Expert - CRA II

ICON Strategic Solutions; Denmark; Vor Ort; DKK 520.000 - 600.000; Vollzeit

Zusammenfassung

ICON Strategic Solutions is seeking a Clinical Research Associate to join our sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

In this CRA II role you will design and monitor trials, ensure data quality and patient safety, and collaborate with investigators across sites while

Qualifikationen

• 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%)

Aufgaben

• Conduct 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

Kenntnisse

Organizational skills

Communication skills

Attention to detail

Team collaboration

Independent work

Travel readiness

Ausbildung

Bachelor's degree in a scientific or healthcare-related field

Tools

ICH-GCP knowledge

Jobbeschreibung

ICON Strategic Solutions is seeking a Clinical Research Associate to join our sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

In this CRA II role you will design and monitor trials, ensure data quality and patient safety, and collaborate with investigators across sites while