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The Senior Clinical Research Associate will oversee and manage clinical trial activities, ensure compliance with protocols and regulations, assess site performance, and provide training and support to site staff.

The Senior Clinical Supply Specialist manages clinical trial supplies' supply chain, ensuring timely delivery and regulatory compliance, while improving logistics and collaborating with clinical teams.

The Manager, Clinical Operations will lead clinical trials, ensuring compliance and operational efficiency, while mentoring junior staff and collaborating with stakeholders.

As a Clinical Research Associate, you will oversee and coordinate clinical trials, ensure regulatory compliance, and analyze research data. You’ll also manage study documentation and build relationships with stakeholders.

The Clinical Research Associate will oversee clinical trial activities, ensure protocol compliance, and manage site relationships to support successful trial execution.

The Project Manager II, Laboratory oversees client inquiries, coordinates studies, manages communication and budgets, develops tools, and represents ICON at client meetings.

The Clinical Trial Liaison develops relationships with trial investigators to facilitate recruitment for clinical trials, ensuring they understand study details and providing strategies for identification of eligible subjects.

The Contract Specialist coordinates, prepares, and executes clinical study contracts, ensuring compliance with GCP/ICH regulations and collaborating with project teams.

As a Clinical Research Associate II, you will conduct site visits for trials, ensure data integrity, collaborate with investigators, and prepare study documents.

The Clinical Trial Assistant will support clinical trials by assisting in planning, execution, monitoring, and maintaining compliance with regulatory guidelines, as well as collaborating with cross-functional teams.