Senior CRA – Lead Monitoring & Site Training

ICON Strategic Solutions; Poland; On-site; PLN 140,000 - 210,000; Full time

Benefits offered by this job

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme,

Life assurance

Flexible country-specific benefits

Job summary

ICON is seeking a Clinical Research Associate to lead monitoring activities for clinical trials, ensuring adherence to protocols and GCP standards. The role involves site visits, issue resolution, and collaboration with cross-functional teams to ensure data quality and timely reporting.

The candidate will train and guide site staff, maintain strong relationships with stakeholders, and travel approximately 60% to sites as required to ensure smooth trial operations.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Extensive experience as a Clinical Research Associate with strong understanding of trial processes and regulatory requirements.
• Proven ability to manage multiple sites and projects with strong organizational and problem-solving skills.
• Expertise in monitoring practices, data integrity, and site management with proficiency in clinical trial tools.
• Excellent communication, interpersonal and stakeholder management skills to drive compliance in a complex environment.
• Willingness to travel as required (approximately 60%).

Responsibilities

• Lead on clinical trial monitoring tasks with focus on quality and continuous improvement.
• Monitor clinical trial sites to ensure adherence to study protocols and GCP standards.
• Conduct site visits to assess performance and resolve issues for successful trial execution.
• Collaborate with cross-functional teams to ensure timely data collection and reporting.
• Provide training and guidance to site staff and other CRAs to maintain high standards of conduct.
• Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth operations.

Skills

Clinical Research

Site monitoring

Regulatory compliance

Data integrity

Communication

Travel coordination

Education

Bachelor's degree

Tools

Clinical trial software

Job description

ICON is seeking a Clinical Research Associate to lead monitoring activities for clinical trials, ensuring adherence to protocols and GCP standards. The role involves site visits, issue resolution, and collaboration with cross-functional teams to ensure data quality and timely reporting.

The candidate will train and guide site staff, maintain strong relationships with stakeholders, and travel approximately 60% to sites as required to ensure smooth trial operations.