Search the 88 jobs at ICON plc

As a Study Start-Up Associate II, you will assist in preparing clinical sites to start trials by reviewing and negotiating contracts, coordinating documentation, facilitating indemnification processes, and mentoring junior staff. You will act as a consultant on study budgets and ensure effective communication with stakeholders.

As a Clinical Research Associate II/Senior CRA, you will conduct site qualifications, ensure protocol compliance, collaborate with investigators, perform data reviews, and contribute to study documentation for clinical trials.

The Payroll Supervisor will oversee the payroll team, ensuring accurate and timely payroll processing, managing relationships with vendors, and handling payroll-related audits. They will coach staff, analyze data, and contribute to process improvements while adhering to compliance and internal controls. The role requires strong administrative skills and a good understanding of payroll best practices.

As a Site Management Associate at ICON, you will manage and monitor clinical studies, ensuring compliance and coordinating with sites. Responsibilities include document collection, electronic Trial Master File management, remote site monitoring, and providing mentorship. You will also support client interactions, clinical budget management, and contribute to business development efforts.

As a Commercial Legal Counsel, you will support ICON's Pharma and Procurement teams in negotiating a variety of commercial contracts. Responsibilities include providing legal advice on contract and compliance issues, managing legal projects, and improving legal processes. You will also liaise with internal stakeholders and external counsel, emphasizing efficiency and value in service delivery.

The Financial Reporting Accountant will ensure timely and accurate financial reporting for two or more entities, maintain statutory compliance, and assist in financial planning. Responsibilities include preparing management accounts, balance sheet reconciliations, and collaborating with auditors and financial advisors.

The Payroll Associate will assist with payroll cycles on a global scale, ensuring accurate inputs for third-party payroll vendors, liaising with HR and Finance, managing the Payroll mailbox, and ensuring compliance with tax and pension requirements. The role requires collaboration with auditors and the Payroll team to improve efficiency and maintain SOX compliance.

As an Accounts Receivable Associate, you will handle invoicing clients, maintaining client relationships, reconciling accounts, and collaborating with internal teams. Requires 2-3 years of experience in a similar role.

As a Clinical Research Associate at ICON, you will independently monitor and set up studies, prepare protocol submissions, manage queries, ensure study cost efficiency, and potentially assist in training fellow CRAs. You will be responsible for adhering to regulatory standards while working on clinical trials in phases II to IV.

The Clinical Trial Administrator at ICON is responsible for coordinating and supporting clinical trials, ensuring compliance with protocols, organizing documentation, preparing study materials, and tracking trial metrics in a collaborative environment.

The Back End Digital Developer is responsible for managing content management systems, back-end development, UAT testing, and analytics setup, particularly with GA4. They collaborate with IT and stakeholders on integration projects and contribute to web development budgets while ensuring timely project delivery with a global team.

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.