Senior CRA: Lead Multi-Site Trials & Quality

ICON Clinical Research; Lisboa; On-site; EUR 60,000 - 76,000; Full time

Benefits offered by this job

Health insurance

Retirement planning

LifeWorks

Global Employee Assistance Programme

Job summary

ICON Strategic Solutions is seeking a Senior Clinical Research Associate to oversee and manage clinical trial activities, ensuring adherence to protocol, regulatory requirements, and industry standards.

You will lead monitoring tasks, conduct site visits, collaborate with cross-functional teams for data collection, and provide guidance to site staff and other CRAs. A strong foundation in trial monitoring and willingness to travel are essential.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Extensive experience as a Clinical Research Associate with knowledge of trial processes.
• Ability to manage multiple sites and projects simultaneously with strong organizational skills.
• Expertise in monitoring practices, data integrity, and site management with relevant software.
• Excellent communication and stakeholder management skills to drive compliance.
• Willingness to travel approximately 60%.

Responsibilities

• Lead clinical trial monitoring tasks with focus on quality and improvement.
• Monitor trial sites for adherence to protocols and GCP.
• Conduct site visits to assess performance and resolve issues.
• Collaborate with cross-functional teams for timely data collection and reporting.
• Provide training to site staff and other CRAs.

Skills

Clinical trial monitoring

GCP compliance

Data integrity

Site management

Stakeholder management

Willingness to travel

Education

Bachelor's degree in a relevant scientific discipline or healthcare-related field

Tools

Clinical trial software

Job description

ICON Strategic Solutions is seeking a Senior Clinical Research Associate to oversee and manage clinical trial activities, ensuring adherence to protocol, regulatory requirements, and industry standards.

You will lead monitoring tasks, conduct site visits, collaborate with cross-functional teams for data collection, and provide guidance to site staff and other CRAs. A strong foundation in trial monitoring and willingness to travel are essential.