Senior Clinical Research Associate - Global Trials & Data

ICON Clinical Research; United Kingdom; Remote; GBP 50,000 - 70,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance

Retirement planning

LifeWorks EAP

Life assurance

Country-specific benefits

Job summary

ICON Strategic Solutions, part of ICON, invites a Senior Clinical Research Associate to join sponsor-dedicated model, supported by ICON’s global expertise. As CRA II, you will design and analyse trials, interpret data, and contribute to development of treatments benefiting patients worldwide.

You will conduct site qualification, initiation, monitoring, and close-out visits, ensure protocol compliance and data integrity, collaborate with investigators and site staff to facilitate study conduct,

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

Organizational skills

Communication skills

Attention to detail

Independent & collaborative work

Travel willingness

Education

Bachelor's degree in science/healthcare

Job description

ICON Strategic Solutions, part of ICON, invites a Senior Clinical Research Associate to join sponsor-dedicated model, supported by ICON’s global expertise. As CRA II, you will design and analyse trials, interpret data, and contribute to development of treatments benefiting patients worldwide.

You will conduct site qualification, initiation, monitoring, and close-out visits, ensure protocol compliance and data integrity, collaborate with investigators and site staff to facilitate study conduct,