Senior Clinical Research Associate

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

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.

- 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.

- Advanced degree in a relevant field such as life sciences, nursing, or medicine.

- 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.

- Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver's license