Senior CRA - Late Phase

Senior CRA - Late Phase

ICON

Warsaw or Gdańsk, Poland

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

What You Will Do:

You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.

Key responsibilities include:

• Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards;
• Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution;
• Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting;
• Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct;
• Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.

Required qualifications and experience:

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