ICON plc

Clinical Research

• Ensures the safety of participants and promotes the mission of Accellacare
• Actively recruits and promotes service to suitable participants and sponsor representatives
• Performs tasks required to coordinate and complete multiple studies according to the protocol
• Assists the Manager of Clinical Operations and Sr. Clinical Research Coordinators with staff development through mentoring and site level quality assurance.
• Performs study start-up duties including the production of a recruitment tool and progress notes
• Proactively develops and executes recruitment plans that meet and exceed enrollment goals
• Accurately collects study data via source documents/progress notes
• Maintains communication with the monitor from the sponsoring company through telephone contact, written communication and on-site visits.

Clinical Research Coordinator

Director

• Leading the strategic planning, development, and implementation of clinical systems, including Electronic Data Capture (EDC), Clinical Trial Management Systems (CTMS), and other technologies supporting clinical trials.
• Overseeing the integration and optimization of clinical systems to ensure seamless data flow, operational efficiency, and compliance with regulatory standards.
• Collaborating with cross-functional teams, including clinical operations, data management, and IT, to define system requirements, address operational challenges, and drive continuous improvement.
• Providing strategic direction on system selection, implementation, and maintenance, ensuring alignment with study objectives, data quality standards, and organizational goals.
• Staying abreast of industry trends and technological advancements to drive innovation in clinical systems and enhance trial management and data analysis capabilities.

Senior Director, Clinical Systems

Data Scientist

• Leading the design, development, and validation of data science programming solutions for clinical trials.
• Collaborating with biostatisticians, data managers, and clinical teams to develop data specifications and analysis plans.
• Programming and validating datasets, tables, listings, and figures (TLFs) according to study requirements.
• Ensuring the accuracy, consistency, and integrity of clinical data through rigorous quality control and validation checks.
• Mentoring and guiding junior programmers and providing technical leadership within the data science programming team.

Lead Clinical Data Science Programmer

Manager

• Leading the development, implementation, and optimization of clinical systems to enhance data collection and reporting processes.
• Collaborating with cross-functional teams to identify system requirements and ensure alignment with clinical trial objectives.
• Monitoring system performance and conducting regular assessments to identify opportunities for improvement and efficiency gains.
• Providing training and support to team members on clinical systems, fostering a culture of proficiency and accountability.
• Building strong relationships with internal stakeholders and technology partners to facilitate effective communication and collaboration on system initiatives.

Manager, Clinical Systems

Analyst

• Leading contract negotiations with clients, vendors, and other stakeholders to establish mutually beneficial agreements.
• Reviewing and analyzing contract terms and conditions to ensure alignment with business objectives and regulatory requirements.
• Providing guidance and support to internal teams on contract interpretation, compliance, and risk mitigation strategies.
• Developing and implementing contract management processes and tools to streamline operations and improve efficiency.
• Collaborating cross-functionally with legal, finance, and operational teams to resolve contract-related issues and disputes.

Senior Contracts Analyst – Part-time 80%

Marketing

• Launch digital advertising through online channels globally to drive patient recruitment for supported clinical studies with a focus in Google and Meta channels
• Monitor and optimize the performance of digital advertising campaigns and assess performance against goals (ROI and KPIs)
• Produce reports and recommendations concerning current and future advertising and patient recruitment strategies
• Liaise with the marketing team on current and upcoming studies, contributing to the formulation of digital outreach strategies
• Provide strategic input to copywriters drafting patient recruitment advertising materials copy and consult with design and production team members to develop images / video assets
• Liaise with study leads on study start-up requirements and during the study enrollment to deliver against randomization targets
• Liaise with media agencies and external vendors to support patient recruitment initiatives

Digital Media Buyer

• Leading the development and implementation of clinical data management strategies to optimize data collection, analysis, and reporting.
• Collaborating with cross-functional teams to ensure the accurate integration of data science techniques into clinical trial designs.
• Overseeing the analysis of clinical data to provide actionable insights that inform study decisions and outcomes.
• Providing strategic guidance on data governance, quality control, and compliance with regulatory requirements.
• Establishing partnerships with key stakeholders to leverage the latest advancements in data science and technology in clinical research.

Senior Clinical Data Science Lead – Sponsor Dedicated

Research Analyst

• Support 4-5 studies at various stages in Orthopedics
• Monitor orthopedic medical device studies
• Identify risks and implement effective solutions promptly
• Communicate effectively with study teams and sites
• Maintain detailed reports on various projects
• Average 65% travel required

Senior Clinical Research Associate – Orthopedics

Customer Support

• Developing and executing project plans, focusing on achieving project goals and objectives.
• Leading cross-functional teams to ensure the successful implementation of project activities.
• Collaborating with stakeholders to identify project requirements and define project scope.
• Mentoring and guiding team members, fostering a culture of excellence and continuous improvement.
• Driving the development of project documentation and reports to present findings to stakeholders in a clear and actionable manner.
• Staying abreast of industry trends and emerging technologies to integrate best practices into project management strategies.
• Contributing to organizational growth through effective project leadership and strategic planning.

Business Support Specialist

• Designing and implementing clinical trial protocols, ensuring adherence to scientific and regulatory standards.
• Conducting data analysis and interpretation to derive insights that support study objectives.
• Collaborating with cross-functional teams to ensure effective study execution and data quality.
• Engaging with stakeholders to communicate findings and contribute to scientific discussions.
• Assisting in the preparation of regulatory submissions, study reports, and scientific publications.

Clinical Scientist

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports.

Clinical Research Associate – Sponsor Dedicated

• Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.
• Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
• Build and manage strong relationships with trial investigators and stakeholders.
• Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.
• Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.

Study Delivery Manager

• Supporting ICON’s rare oncology focused biotech and pharmaceutical clients to develop and implement a strong patient advocacy strategy and to incorporate the patient voice into the clinical development lifecycle.
• Working closely with patient advocacy organizations, biotech and pharmaceutical industry clients, as well as internal ICON teams and stakeholders.
• Interacting with client’s teams and ICON internal teams to ensure the perspective, needs, and challenges faced by rare oncology diseases are considered and incorporated into protocol reviews and study conduct planning.
• Functioning as an extension of the client’s team to identify key relevant patient advocacy organizations, develop an engagement strategy and implement through direct liaison.
• Supporting the Patient Advocacy team as a rare oncology disease patient advocacy strategy SME.
• Working closely with client teams, developing and implementing patient advocacy strategies and engagement on behalf of ICON’s clinical stage, rare oncology disease focused clients aligned to client’s clinical development strategy.
• Serving as a patient advocacy strategy SME in protocol reviews, study conduct planning meetings, proposal development and client meetings.
• Developing patient-focused thought leadership content.

Director, Patient Advocacy – Rare Oncology Disease

Project Manager

• Developing and managing detailed project plans, including timelines, budgets, and resource allocation to ensure successful project delivery.
• Leading cross-functional project teams, coordinating efforts to meet project objectives, and facilitating effective communication and collaboration.
• Monitoring project progress, identifying potential risks and issues, and implementing strategies to address challenges and keep projects on track.
• Engaging with stakeholders to manage expectations, provide updates, and ensure alignment with project goals and organizational objectives.
• Preparing and presenting project reports, status updates, and performance metrics to senior management and other stakeholders.

Software Engineer

• Be responsible to function in a continuous improvement framework with respect to systems deployment, life cycle management and enhancements supported user groups.
• Contribute to initiatives to yield faster and more effective report development, efficient change management services for analytics platforms.
• Use your technical expertise with clinical data and report building, and experience gained through working with diverse and complex business processes and associated system infrastructures.
• Work in a matrix environment across functions and departments