Senior Clinical Research Associate — Lead Global Trials

ICON Clinical Research

Lisboa

On-site

EUR 42,000 - 65,000

Full time

5 days ago

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Job summary

ICON Clinical Research is seeking a Senior Clinical Research Associate to oversee clinical trial monitoring, ensuring adherence to protocol, regulatory requirements, and GCP standards. You will lead on monitoring tasks, conduct site visits, and collaborate with cross-functional teams to ensure data quality and trial success.

The role requires extensive CRA experience, strong communication, and the ability to travel ~60% to support site activities across regions.

Qualifications

Bachelor's degree in a relevant scientific discipline or healthcare-related field.
Extensive experience as a Clinical Research Associate with strong regulatory knowledge.
Proven ability to manage multiple sites and projects with strong organizational skills.
Expertise in monitoring practices, data integrity, and site management with proficiency in trial software.
Excellent communication and stakeholder management skills; willingness to travel approx. 60%

Responsibilities

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and 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.