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The Disclosure Specialist supports clinical trial transparency, focusing on document redaction, results posting, and ensuring compliance with global regulations while collaborating with various teams.

The Project Manager will lead project activities, ensuring timely and budget-compliant delivery while managing cross-functional teams and stakeholder communication.

The Clinical Trial Recruitment Representative recruits study subjects for clinical trials, manages phone screenings, maintains databases, and supports the recruiting team to meet volunteer requirements.

The CRA I will conduct clinical trial monitoring, coordinate study activities, maintain documentation, and ensure compliance with ICON's procedures. This role includes developing relationships with stakeholders and ensuring patient safety.

Responsible for processing and payment of invoices, reconciliation of accounts, and resolution of supplier and employee queries.

As a Senior Contract Analyst, you'll manage contracts, ensuring compliance and guidance on regulatory requirements, while mentoring colleagues and supporting project teams.

The Senior Clinical Research Associate will conduct monitoring visits for clinical trials, ensuring compliance, data integrity, and patient safety while collaborating with investigators and preparing study documentation.

As a CRA II, you'll monitor clinical trials, ensuring compliance and data integrity, while collaborating with site staff and preparing study documentation.

The Project Manager will oversee clinical trial activities, ensuring timely delivery, quality standards, and regulatory compliance while managing country and site level operations.

As a Contract Analyst at ICON, you will manage invoicing processes, maintain client relationships, reconcile accounts, and collaborate with the Revenue team.