Global CRA II: Trial Monitoring & Data Integrity

ICON Docs division Malaysia; Kuala Lumpur; Vor Ort; MYR 90.000 - 150.000; Vollzeit

Benefits dieser Stelle

Health and wellbeing programmes

Retirement plans

Life assurance

Zusammenfassung

ICON Strategic Solutions in Kuala Lumpur is seeking a Clinical Research Associate II to monitor clinical trials and ensure data integrity across sites. You will design and analyse trial activities, interpret complex medical data, and contribute to the advancement of therapies that benefit patients worldwide.

The role requires conducting site qualification, initiation, monitoring, and close-out visits, ensuring protocol compliance and data quality, and collaborating with investigators.

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

• 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

Kenntnisse

Strong organizational andcommunication

Attention to detail

Independent and collaborative work

Willingness to travel

Ausbildung

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

Tools

ICH-GCP knowledge

Jobbeschreibung

ICON Strategic Solutions in Kuala Lumpur is seeking a Clinical Research Associate II to monitor clinical trials and ensure data integrity across sites. You will design and analyse trial activities, interpret complex medical data, and contribute to the advancement of therapies that benefit patients worldwide.

The role requires conducting site qualification, initiation, monitoring, and close-out visits, ensuring protocol compliance and data quality, and collaborating with investigators.