Search the 123 jobs at ICON plc

The Senior Contract Analyst at ICON will manage contractual agreements, ensuring compliance and alignment with regulatory requirements. Responsibilities include drafting and negotiating contracts, analyzing contract terms for risks and opportunities, maintaining contract records, and developing contract management processes.

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 Senior Contract Analyst, you will manage contractual agreements, ensuring compliance and supporting project teams with contract interpretation and obligations. Your role includes reviewing, drafting, and negotiating contracts while maintaining organized records and improving contract management processes.

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 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.

As a Study Support Assistant, you will assist in preparing and submitting regulatory documents, coordinate with stakeholders for approvals, maintain records of submissions, support study teams in developing study documents, and participate in study start-up meetings.

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.

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 Site Activation Lead will oversee the startup activities of clinical trials, ensure contract teams meet deadlines, and manage negotiations while maintaining communication with stakeholders. Responsibilities include developing country and site distribution plans, leading sponsor initiatives, and mentoring junior associates. Requires excellent project management and communication skills.

The Senior Site Activation Lead will manage global or multi-regional large-scale studies, acting as the main contact for stakeholders, overseeing the start-up strategy, supporting project management tasks, and managing risks throughout the study start-up phase.

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.

As a Clinical Trial Administrator at ICON, you will assist in coordinating clinical trials, ensure compliance with protocols, maintain documentation, support materials preparation, and contribute to tracking trial metrics.

As an IHCRA at ICON, you will assist in planning, initiating, and executing clinical trial activities, conduct site assessments, ensure compliance with study protocols, monitor study progress, and assist in preparing study documentation.

As a Study Support Assistant, you will assist in the study startup process by providing administrative and tracking support, managing submission documentation, and updating relevant tracking systems. You'll also coordinate meetings and assist with the coordination of payments while ensuring adherence to ICH GCP and ICON SOPs.

The Study Start Up Associate II reviews and negotiates Informed Consent Forms (ICF) while liaising with stakeholders like sponsors and legal teams. They also assist in creating country-specific ICF templates for clinical trials in the United States and Canada, ensuring compliance with local requirements.

The Site Activation Lead is responsible for overseeing contracts and budgets, managing study progression, conducting template builds and reviews, and facilitating escalations within internal departments and with clients in the context of clinical trials.

The Project Assistant will support the team in managing multiple clinical trials, handling administrative tasks, project reports, and communications with clients and stakeholders. Duties include scheduling meetings, maintaining study files, managing study supplies, and assisting with audit preparations.

The Clinical Research Associate II Specialist will conduct site visits for clinical trials, ensuring compliance with protocols and data integrity while collaborating with investigators. Responsibilities also include data review, resolution of queries, and assisting in the preparation of study documentation.

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 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.