ICON plc

www.iconplc.com

2 Jobs

37,004 Employees

About the Company

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times.

We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.

Listed Jobs

Company Name: ICON plc
Job Title: Senior Software Engineer
Job Description: **Job Title:** Senior Software Engineer **Role Summary:** Lead the design, development, and maintenance of SaaS Medical Publishing solutions using Microsoft .NET/C#, MVC, SQL Server, and REST APIs. Own technical ownership of projects, collaborate with cross‑functional teams, and serve as the primary technical liaison with clients. **Expectations:** - Deliver high‑quality code within agreed timelines. - Own planning, execution, and troubleshooting of assigned tasks. - Communicate status, risks, and solutions clearly to stakeholders. **Key Responsibilities:** - Design, code, unit‑test, and deploy software components with minimal supervision. - Write detailed technical specifications and database schemas. - Conduct code and design reviews; propose system improvements. - Lead client demonstrations and manage technical aspects of client calls. - Collaborate with development, QA, and client service teams to ensure seamless integration. - Participate in Agile ceremonies (sprint planning, stand‑ups, retrospectives). - Offer assistance to teammates, fostering a collaborative environment. - Update project schedules and report progress to management. **Required Skills:** - 6+ years of progressive software development experience in Microsoft .NET/C#, MVC, SQL Server, REST APIs, and Visual Studio. - Advanced SQL: database design, complex queries, stored procedures, and views. - JavaScript/JSON, AJAX, HTML, CSS, jQuery – ability to build responsive UI components. - OOP principles, design patterns, and solid architecture practices. - Familiarity with SaaS delivery models and Azure DevOps pipelines. - Experience with TortoiseSVN version control. - Minimum 2 years of Power BI analytics development. - Agile development experience (Scrum/Kanban). - Strong analytical, problem‑solving, and independent work capabilities. - Excellent communication skills – able to translate technical concepts to non‑technical stakeholders. **Required Education & Certifications:** - Bachelor’s or Master’s degree in Computer Science, Software Engineering, or a related field.

Reading, United kingdom

Remote

Senior

18-11-2025

Company Name: ICON plc
Job Title: Clinical Research Associate
Job Description: **Job title:** Clinical Research Associate II / Senior Clinical Research Associate **Role Summary:** Independent monitor of Phase II–III clinical trials for small and mid‑sized biopharma sponsors. Conduct site qualification, initiation, monitoring and close‑out visits; ensure compliance with ICH‑GCP, regulatory and local requirements; manage study documentation, ethics approvals and regulatory submissions; mentor junior CRAs; oversee study cost efficiency and issue resolution; operate across oncology and other therapeutic areas in France. **Expectations:** - 2 + years experience as CRA II or 4 + years as Senior CRA. - Residency in Paris or Lyon; professional travel within France. - Fluency in French and professional proficiency in English. - Ability to work independently, manage multiple studies, and drive on‑time, budget‑conscious deliverables. **Key Responsibilities:** - Monitor sites (qualification, initiation, ongoing monitoring, close‑out) for Phase II–III studies. - Ensure adherence to ICH‑GCP, national regulations, sponsor SOPs, and study protocols. - Manage and maintain accurate site documentation, including trial master file and regulatory files. - Prepare and submit regulatory/ethics documentation and updates. - Collaborate with cross‑functional teams (data management, safety, biostatistics) and site staff to resolve issues and maintain data quality. - Mentor and coach site personnel and junior CRAs. - Track study cost performance; identify and resolve budget variances. - Coordinate and support site meetings, training, and investigator meetings. - Contribute to study planning and design consultations as needed. **Required Skills:** - Strong knowledge of ICH‑GCP, EMEA, and local French regulations. - Excellent written and verbal communication in French and English. - Proficiency with clinical trial systems (e.g., Medidata Rave, OpenClinica) and MS Office. - Good organizational, problem‑solving and analytical skills. - Ability to travel within France and work independently. - Leadership potential for mentoring junior staff. **Required Education & Certifications:** - Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field (or equivalent). - No mandatory certifications, though CRCT, GCP or similar training is highly advantageous.