Search the 99 jobs at ICON plc

The Quality Control Analyst II is responsible for sustaining the global quality control program, conducting data management and analysis, supporting internal audits, and ensuring regulatory compliance. The role involves effective communication, collaboration with laboratory personnel, and driving quality improvement initiatives.

As a Clinical Research Associate (CRA) at ICON, you'll independently monitor clinical studies, ensuring compliance with regulations, managing documentation, and facilitating study start-up and close-out processes. You will also handle regulatory submissions and assist in training fellow CRAs while contributing to study cost efficiency.

The Finance Manager oversees a team of financial accountants, ensuring accurate financial reporting and compliance with statutory requirements. Responsibilities include delivering management accounts, maintaining balance sheet reconciliations, developing team performance, and assisting the Finance Director in global financial accounting processes.

As a Group Financial Accountant at ICON plc, you will be responsible for external reporting, monthly consolidation processes, quarterly and annual filings, and collaborating with various teams to support financial control and reporting. The role requires strong attention to detail and the ability to streamline processes in a large organization.

The Commercial Finance Analyst will support global financial control, collaborating with clients to tailor commercial terms, preparing budgets for proposals, and ensuring proposals are financially sound. The role also involves coordinating with various departments and maintaining accurate records while managing multiple tasks.

The Proposals Development Associate II role at ICON involves preparing high-quality client-focused proposals and budgets for clinical trials, coordinating proposal processes, participating in client meetings, and ensuring timely submissions. This position is critical for supporting business development efforts and requires interaction with various operational departments to align proposals with business needs.

The Study Start Up Associate II will lead the preparation and submission of regulatory documents for clinical trials, coordinate with stakeholders for necessary approvals, manage regulatory submission records, and support study teams on regulatory guidelines and process improvements.

As a Contract Analyst II at ICON, you'll review and analyze contracts related to clinical trials, negotiate terms, collaborate with teams to assess and mitigate contract risks, and maintain accurate records in contract management systems. You will also provide guidance on contract-related matters.

The Study Start Up Associate I & II assists in executing site activation for clinical trials, ensuring compliance with project timelines and requirements. Responsibilities include overseeing site progress, supporting tool maintenance, and participating in study reviews to identify risks.

As a Clinical Research Associate at ICON Plc, you will oversee and coordinate clinical trials, ensuring compliance with regulations and analyzing data. Responsibilities include setting up studies, maintaining documentation, and fostering relationships with stakeholders to ensure patient safety and efficient study management.

As a Statistical Analyst, you will support clinical trial activities by contributing to study designs, writing statistical methods sections, developing statistical analysis plans, and programming statistical procedures using SAS, along with creating project reports and maintaining client communication.

The Site Identification Specialist I will work with the Site Identification Lead to identify potential study sites and investigators for clinical trials, ensuring high-quality data collection and site evaluation. Responsibilities include building relationships with sites, performing phone visits, liaising with country managers, and maintaining compliance with procedures and documentation.

As a Global Feasibility Manager, you will lead the clinical project feasibility process, assist Business Development with cost proposals, and support strategic partnerships. You will be a technical expert in feasibility for clients and manage the delivery of awarded projects effectively.

As a Study Start Up Associate I/II, you will assist in preparing and submitting regulatory documents, coordinate with stakeholders for study approvals, maintain accurate records, support study teams in document development, and participate in startup meetings to provide input on regulatory requirements and timelines.

As the Accounts Receivable Manager, you will oversee a global team, ensuring efficient accounts receivable processes, managing billing, coordinating audits, and fostering a high-performance team culture focused on continuous improvement and client relationships.

The Senior Technical Project Manager will lead the planning, execution, and delivery of complex technical projects for clinical research operations while ensuring alignment with business objectives and effective communication across cross-functional teams.

The Senior Data Analyst will analyze data related to quality and compliance in clinical trials. The role involves interpreting data, reporting insights to support decision-making, and managing strategic initiatives involving data analytics and AI in a QA context. The successful candidate will work closely with stakeholders to drive improvements.

The RFI Specialist Associate will manage and prepare Requests for Information (RFIs) accurately and timely, draft responses, collaborate with team members, and maintain the RFI Content Library. This role requires strong communication, organizational, and problem-solving skills, along with the ability to work under tight deadlines.

As a Proposals Development Associate II, you will lead the preparation of client proposals, collaborate with cross-functional teams to gather information, conduct research and analysis on market trends, manage the proposal workflows, and maintain proposal documents and tools.

The Senior Financial Accountant (Accounts Receivables) will manage timely processing of invoices and support the AR team. Responsibilities include conducting reviews of AR processes, improving operational efficiency, handling dispute invoices, and ensuring compliance with internal controls and regulations.