Clinical Research Associate II - Global Trials (60% Travel)

Regulatory Jobs; Center Square (PA); On-site; USD 70,000 - 100,000; Full time

Benefits offered by this job

Competitive base salary

Health and wellbeing programmes

Retirement and pension plans

Life assurance and disability coverage

Employee assistance programmes andWell

Wellbeing resources

Learning and development opportunities

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate II to join a sponsor-dedicated model supported by ICON’s global expertise. You will design and analyse clinical trials, interpret complex medical data, and contribute to the advancement of therapies that benefit patients worldwide.

In this CRA II role, you will conduct site visits, ensure protocol compliance, and collaborate with investigators to maintain high-quality data and study documentation. Travel up to ~60% is required.

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

• 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

Clinical trial monitoring

ICH-GCP knowledge

Attention to detail

Communication skills

Travel willingness

Education

Bachelor's degree in science/healthcare

Job description

ICON Strategic Solutions is seeking a Clinical Research Associate II to join a sponsor-dedicated model supported by ICON’s global expertise. You will design and analyse clinical trials, interpret complex medical data, and contribute to the advancement of therapies that benefit patients worldwide.

In this CRA II role, you will conduct site visits, ensure protocol compliance, and collaborate with investigators to maintain high-quality data and study documentation. Travel up to ~60% is required.