CRA II: Clinical Trials Monitoring in Helsinki

ICON Strategic Solutions; Helsinki; Vor Ort; EUR 42.000 - 65.000; Vollzeit

Benefits dieser Stelle

Health insurance

Retirement planning

Employee assistance program

Life assurance

Zusammenfassung

ICON Strategic Solutions in Helsinki is seeking a Clinical Research Associate II to contribute to sponsor-dedicated trials, backed by ICON’s global expertise. As the world’s largest FSP, ICON offers stability, career development and a collaborative environment advancing treatments that benefit patients worldwide.

You will conduct site qualification, initiation, monitoring and close-out visits, ensure protocol compliance, data integrity and patient safety, and collaborate with investigators to

Qualifikationen

• Bachelor's degree in a scientific or healthcare field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• 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

Ausbildung

Bachelor's degree in scientific/healthcare field

Jobbeschreibung

ICON Strategic Solutions in Helsinki is seeking a Clinical Research Associate II to contribute to sponsor-dedicated trials, backed by ICON’s global expertise. As the world’s largest FSP, ICON offers stability, career development and a collaborative environment advancing treatments that benefit patients worldwide.

You will conduct site qualification, initiation, monitoring and close-out visits, ensure protocol compliance, data integrity and patient safety, and collaborate with investigators to