Senior Clinical Research Associate | Remote Trials Leader

KCR Placement; Center Square (PA); Remote; USD 70,000 - 90,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Job summary

ICON is seeking a Senior Clinical Research Associate or Clinical Research Associate II for the US-Remote role. You will design and analyze clinical trials, interpret complex medical data, and support the advancement of innovative treatments and therapies.

Responsibilities include site visits, data review, and collaboration with investigators to ensure high-quality trial conduct while maintaining patient safety and protocol compliance. Travel up to 60% is required (domestic and international).

Qualifications

• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Bachelor's degree in a scientific or healthcare-related field.
• Excellent organisational and communication skills with attention to detail.

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 reports.

Skills

Organisational skills

Communication skills

Travel readiness

Independent work

Education

Bachelor's degree in science/healthcare

Job description

ICON is seeking a Senior Clinical Research Associate or Clinical Research Associate II for the US-Remote role. You will design and analyze clinical trials, interpret complex medical data, and support the advancement of innovative treatments and therapies.

Responsibilities include site visits, data review, and collaboration with investigators to ensure high-quality trial conduct while maintaining patient safety and protocol compliance. Travel up to 60% is required (domestic and international).