The Senior Pharmacovigilance Associate is responsible for managing pharmacovigilance activities, including the evaluation of adverse event reports, data analysis, preparation of safety reports, and ensuring regulatory compliance. The role involves collaboration with medical teams and mentoring junior staff, all while maintaining patient safety and data integrity.

As a Senior Pharmacovigilance Associate, you will manage pharmacovigilance activities, evaluate adverse event reports, analyze safety data, prepare regulatory documents, and collaborate with cross-functional teams on patient safety and compliance. You'll also mentor junior team members and stay updated on regulatory guidelines.

As a Principal Biostatistician at ICON, you will lead statistical activities for clinical trials, oversee statistical methods in protocols, and prepare research proposals. You will also participate in meetings with clients and regulatory bodies, contributing to clinical development and innovative therapies.

As a Contract Analyst II, you will coordinate and develop contracts and change orders, manage multiple projects, communicate with various teams, and ensure the quality of contract submissions. Your role will involve building relationships internally and externally, providing financial analysis, and improving processes within the organization.

The Senior Clinical Research Associate (CRA) position involves overseeing clinical trial activities, ensuring compliance with protocols, conducting site visits, and collaborating with teams for accurate data collection. The CRA will provide training to site staff, manage multiple sites, and maintain relationships with stakeholders to ensure successful trial execution.

As a Senior Clinical Research Associate at ICON, you'll conduct site qualifications, monitor clinical trials, ensure compliance with protocols, collaborate with investigators, and maintain high-quality clinical data while supporting innovative treatments.

The Senior Pharmacovigilance Associate manages pharmacovigilance activities, ensures compliance with regulatory requirements, leads data analysis, prepares safety reports, and collaborates with cross-functional teams. This role also includes mentoring junior staff and engaging in audits to maintain patient safety and data integrity.

The Biostatistician II will plan, monitor, organize, and review biostatistics and programming activities for moderate complexity studies, ensuring timely and budget-compliant delivery. Responsibilities include protocol input, statistical analysis plans, data interpretation, and writing statistical methods sections for reports.

The Technical Data Analyst at ICON supports Imaging Science, Project Management, and Radiology by reviewing and approving image analyses for data delivery. Responsibilities include identifying data entry errors, quality control of source documents, ensuring timely resolution of errors, and participating in team meetings. A background in imaging and knowledge of clinical trials within a regulated environment is preferred.

The Senior Research Scientist will work on Flow Cytometry and Flow Assays, focusing on method development, experiment design, and quality execution. The role includes mentoring junior scientists, maintaining scientific knowledge, analyzing samples, and ensuring compliance with regulations.

As an Account Executive, you will manage client relationships, identify growth opportunities, collaborate with teams to create tailored solutions, oversee project timelines and budgets, and provide updates to clients on project outcomes.

As a TMF Specialist, you will manage and process clinical study documents, ensure compliance with regulations, and maintain study files. Responsibilities include liaising with study teams, completing departmental projects, quality control of documents, and participating in audits. This role supports both client services and internal needs.

The Associate Project Manager will ensure client satisfaction in managing ICON's Central Laboratories services. The role includes project coordination, adherence to protocols, communication with stakeholders, and monitoring study budgets. Other responsibilities include preparing management reports, representing ICON in meetings, and mentoring junior team members.

As a Data Analyst, you will elicit and document business requirements, translate them into functional UML models, create application report specifications, collaborate with cross-functional teams, estimate requirement efforts, and manage small-to-medium projects while ensuring data compliance and quality.

As Director of Global Supply Chain at ICON, you will oversee S&OP processes, lead integration of new studies, implement forecasting and capacity planning systems, and analyze data to support decision-making and drive continuous improvement. You will also manage Vendor Managed Inventory for clinical sites and ensure delivery performance.

The HR Manager will support country leadership and site heads in Italy and other countries, handling HR activities, employee relations, compliance, and communication. They will be responsible for implementing HR strategies and analyzing key trends to improve workforce management while collaborating with management teams on various HR-related initiatives.

The Business Development Coordinator will assist in developing strategic plans, conduct market research, prepare proposals and presentations, manage client relationships, and collaborate with internal teams to meet client needs effectively.

The PK Scientist will design and conduct quantitative pharmacology studies, prepare regulatory summaries, and present scientific publications, while building relationships with clients. The role emphasizes excellent organizational and communication skills, with a focus on model-based strategies for clinical development.

As a Senior Clinical Research Associate at ICON, you will manage clinical trials, ensuring adherence to protocols and data integrity, while collaborating with site staff and investigators. Responsibilities include site visits, monitoring compliance, and assisting in study documentation.

The Front Desk Administrative Assistant provides support within a Phase 1 Research Clinic, managing front desk operations, data entry, and communication. Responsibilities include coordinating meetings, managing travel, documenting reports, and maintaining relationships with associates and management, all while adhering to company values and processes.