Clinical Research Associate II – Trial Monitoring

ICON Strategic Solutions; Vancouver; On-site; CAD 70,000 - 110,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

LifeWorks EAP

Life assurance

Flexible benefits

Job summary

ICON Strategic Solutions in Vancouver is seeking a Clinical Research Associate II to contribute to sponsor-dedicated trials. You will design and analyze trials, monitor sites, ensure data integrity, and support the preparation of study documentation.

This role requires a bachelor's degree in a scientific field, at least 2 years CRA experience, knowledge of ICH-GCP, strong organizational skills, travel up to 60%, and the ability to work both independently and with investigators.

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%).

Responsibilities

• 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

Skills

Organizational skills

Communication skills

Attention to detail

Independent work

Travel readiness

Education

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

Job description

ICON Strategic Solutions in Vancouver is seeking a Clinical Research Associate II to contribute to sponsor-dedicated trials. You will design and analyze trials, monitor sites, ensure data integrity, and support the preparation of study documentation.

This role requires a bachelor's degree in a scientific field, at least 2 years CRA experience, knowledge of ICH-GCP, strong organizational skills, travel up to 60%, and the ability to work both independently and with investigators.