Senior CRA – Remote Late-Phase Monitoring Leader

ICON Clinical Research; Warszawa; Remote; PLN 180.000 - 260.000; Vollzeit

Benefits dieser Stelle

Annual leave

Health insurance

Retirement planning

LifeWorks support

Life assurance

Flexible benefits

Zusammenfassung

ICON Plc is seeking a Senior Clinical Research Associate for a home-based role in Poland. You will monitor clinical trial sites, ensure protocol and GCP compliance, and collaborate with cross-functional teams to ensure timely data capture.

The role requires extensive CRA experience, strong regulatory knowledge, and the ability to travel up to 60%. We offer a competitive benefits package and inclusive culture.

Qualifikationen

• Bachelor's degree in a relevant scientific or healthcare field.
• Extensive experience as a Clinical Research Associate with regulatory knowledge.
• Ability to manage multiple sites and projects.
• Proficiency in monitoring practices and data integrity.
• Excellent communication and stakeholder management.
• Willingness to travel about 60%.

Aufgaben

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

Kenntnisse

CRA experience

Clinical monitoring

Regulatory knowledge

Data integrity

Site management

Travel readiness

Ausbildung

Bachelor's degree in life sciences

Tools

EDC systems

CTMS

Jobbeschreibung

ICON Plc is seeking a Senior Clinical Research Associate for a home-based role in Poland. You will monitor clinical trial sites, ensure protocol and GCP compliance, and collaborate with cross-functional teams to ensure timely data capture.

The role requires extensive CRA experience, strong regulatory knowledge, and the ability to travel up to 60%. We offer a competitive benefits package and inclusive culture.