Senior CRA: Lead Site Monitoring & Trial Oversight

ICON Strategic Solutions; Reading; On-site; GBP 55,000 - 75,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

Global EAP LifeWorks

Life assurance

Flexible country-specific benefits

Job summary

ICON Strategic Solutions is seeking a Senior Clinical Research Associate (SrCRA) to oversee and manage clinical trial activities in Reading, UK. You will monitor sites to ensure adherence to protocols and GCP, travel up to 60%, and collaborate with cross-functional teams to ensure accurate data collection and reporting.

The role emphasizes independent work, training, and guidance to site staff, with a path to contribute to global sponsor-dedicated programs within ICON’s extensive network.

Qualifications

• Bachelor's degree in a scientific/healthcare field.
• Extensive experience as a Clinical Research Associate and strong regulatory understanding.
• Ability to manage multiple sites and projects with strong organizational skills.
• Expertise in monitoring, data integrity and site management; proficient in clinical trial tools.
• Excellent communication and stakeholder management; able to influence in complex environments.
• Willingness to travel approximately 60%.

Responsibilities

• Lead on clinical trial monitoring tasks with focus on quality and improvement.
• Conduct site visits to assess performance and resolve issues.
• Collaborate with cross-functional teams for timely data collection and reporting.
• Provide training and guidance to site staff and other CRAs.
• Build and maintain relationships with site personnel and stakeholders.

Skills

Clinical monitoring

Multisite management

Data integrity

Regulatory knowledge

Communication skills

Travel flexibility

Education

Bachelor's degree in a relevant scientific discipline

Tools

Clinical trial software

Job description

ICON Strategic Solutions is seeking a Senior Clinical Research Associate (SrCRA) to oversee and manage clinical trial activities in Reading, UK. You will monitor sites to ensure adherence to protocols and GCP, travel up to 60%, and collaborate with cross-functional teams to ensure accurate data collection and reporting.

The role emphasizes independent work, training, and guidance to site staff, with a path to contribute to global sponsor-dedicated programs within ICON’s extensive network.