Senior CRA: Global Trial Monitoring & Site Leadership

ICON Strategic Solutions; United States; On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

Life assurance

Global EAP LifeWorks

Job summary

ICON Strategic Solutions is seeking a Senior Clinical Research Associate to oversee trial activities in a sponsor-dedicated model, ensuring compliance with protocol, regulatory requirements, and GCP. You will lead monitoring tasks, conduct site visits, collaborate with cross-functional teams to ensure timely and accurate data collection, and train site staff to uphold high standards.

The role requires strong independence, multi-site management, excellent communication, and willingness to travel

Qualifications

• Bachelor's degree in a scientific or healthcare field.
• Extensive experience as a Clinical Research Associate with knowledge of trial processes.
• Ability to manage multiple sites and projects and solve problems.

Responsibilities

• Monitor clinical trial sites to ensure adherence to protocols, regulatory requirements and GCP.
• Conduct site visits to assess performance and resolve issues for successful trial execution.
• Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting.
• Provide training and guidance to site staff to maintain high standards of conduct.
• Build and maintain relationships with site personnel and stakeholders to facilitate smooth operations.

Skills

Clinical trial monitoring

Regulatory compliance

Site management

Stakeholder management

Travel coordination

Education

Bachelor's degree in a relevant scientific field

Tools

Clinical trial software

Job description

ICON Strategic Solutions is seeking a Senior Clinical Research Associate to oversee trial activities in a sponsor-dedicated model, ensuring compliance with protocol, regulatory requirements, and GCP. You will lead monitoring tasks, conduct site visits, collaborate with cross-functional teams to ensure timely and accurate data collection, and train site staff to uphold high standards.

The role requires strong independence, multi-site management, excellent communication, and willingness to travel