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The Clinical Research Associate II conducts monitoring and close-out visits, ensures protocol compliance, and collaborates with site staff for clinical trials. They analyze data and maintain high-quality clinical records.

The Clinical Research Associate oversees clinical trials, ensuring compliance, coordinating activities, and maintaining study documentation while developing stakeholder relationships.

As a Commercial Legal Counsel at ICON, you will negotiate contracts, advise on legal issues, manage projects, and support various stakeholders in the pharmaceutical industry.

As a Senior CRA, you'll monitor clinical trial sites, ensure regulatory compliance, collaborate with teams, and train site staff to maintain standards.

The Clinical Research Associate II role involves conducting clinical trial visits, ensuring compliance, facilitating collaboration with site staff, maintaining data integrity, and preparing study documentation.

The Clinical Trial Liaison will improve clinical research site experiences by connecting with investigators, managing site selection, providing training, and monitoring performance indicators. This role requires understanding regulatory requirements and maintaining relationships with clinical sites.

The candidate will manage site relationships, oversee clinical trial operations, ensure compliance, and collaborate with teams to optimize trial performance.

The Senior Clinical Research Associate will oversee clinical trial activities, ensuring compliance with protocols and regulations, while managing site performance and providing support.

The Clinical Research Associate II will conduct site monitoring and ensure compliance during clinical trials, focusing on data integrity and patient safety.

The SSU Lead Specialist will drive study initiation by conducting feasibility assessments, negotiating site contracts, and ensuring regulatory compliance for clinical trials.