Clinical Research Associate II — Trials & Sites

ICON Strategic Solutions; Malaysia; On-site; MYR 70,000 - 95,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Life assurance

Retirement planning

Global EAP LifeWorks

Job summary

ICON Strategic Solutions is seeking a CRA II to support sponsor-dedicated trials with global expertise. You will design and analyse trials, interpreting complex medical data to contribute to treatments that benefit patients worldwide.

You will conduct site visits, ensure protocol compliance and data integrity, collaborate with investigators, and review study documentation while traveling up to 60% for trial activities.

Qualifications

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

Responsibilities

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

Skills

Independence

Teamwork

Travel readiness

Attention to detail

Clinical Trial knowledge

Education

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

Job description

ICON Strategic Solutions is seeking a CRA II to support sponsor-dedicated trials with global expertise. You will design and analyse trials, interpreting complex medical data to contribute to treatments that benefit patients worldwide.

You will conduct site visits, ensure protocol compliance and data integrity, collaborate with investigators, and review study documentation while traveling up to 60% for trial activities.