Responsible for the accurate and timely reporting of safety data, preparing regulatory documents, analyzing trends, and ensuring compliance in pharmacovigilance.

As a Statistical Programmer, you'll analyze clinical trial data, create ADaM datasets, and develop statistical programs while ensuring compliance with regulatory standards.

Analyze clinical trial data and support statistical analysis by developing and validating statistical programs while ensuring regulatory compliance.

The role involves assisting in clinical trial activities, conducting site assessments, ensuring compliance, monitoring study progress, and preparing documentation.

Manage study documents, provide administrative support to project teams, organize meetings, maintain timelines, and support project financial tasks.

As a Pharmacovigilance Associate, you will monitor pharmaceutical safety by analyzing reports, conducting risk assessments, and collaborating with teams to maintain compliance.

The Logistics Specialist will manage logistics processes for clinical trials, ensuring efficient flow of materials, compliance, and collaboration with teams and vendors.

The Site Management Associate I supports clinical trial site management through monitoring activities, ensuring protocol compliance, and providing administrative support.

The Vice President of Business Development will lead strategic initiatives, develop business strategies, pursue partnerships, and direct a business development team.

The Manager of Study Start-Up oversees clinical trial initiation activities, manages a team, ensures compliance, and drives process improvement.

The Senior Clinical Trial Assistant will provide administrative support, manage documentation, and coordinate clinical trial operations while ensuring compliance with regulatory requirements.

Lead and oversee study start-up activities for clinical trials, managing a team and ensuring compliance with regulations.

Perform site qualification, monitor clinical trials, ensure protocol compliance, and maintain data integrity while collaborating with site staff.

Support project managers in coordinating clinical trials, manage study activities, and assist in data analysis for effective decision-making.

The Senior Statistician will support clinical studies, perform statistical analysis, design case report forms, and collaborate with teams to interpret data results.

As a Senior Clinical Research Associate (CRA), you will oversee clinical trial activities, ensuring compliance with protocols and regulatory standards while managing sites and fostering stakeholder relationships.

As a Clinical Research Associate II, you will conduct site visits, ensure protocol compliance, and review clinical data while collaborating with investigators.

As a Senior Auditor Quality Assurance at ICON, you will conduct audits of clinical trial processes, collaborate with teams, develop audit plans, provide guidance on best practices, and improve quality assurance initiatives.

As an In-House Clinical Research Associate, you will assist in planning, coordinating, and executing clinical trial activities ensuring compliance with protocols and quality standards.

As a Principal Biostatistician, you will design and analyze clinical trials, oversee statistical activities, and contribute to innovative treatments.