Search the 25 jobs at ICON plc

Become familiar with ICON's SOPs, assist with investigator recruitment, maintain data accuracy, serve as primary contact for sites, conduct remote site management, participate in QA Audits, and more.

As a Study Start Up Associate II at ICON, you will play a vital role in preparing physicians at research sites for clinical trials of new pharmaceutical and biological products. Responsibilities include reviewing and negotiating contracts, tracking critical documents, and facilitating the indemnification process. A bachelor's degree in Paralegal Studies, Juris Doctor degree, or related experience is preferred. SSU experience is desirable but not required. Competitive salary packages, health-related benefits, and retirement plans are offered, along with a culture that rewards high performance and nurtures talent.

As a Senior Clinical Research Associate at ICON, you will be responsible for setting up and monitoring studies, submitting regulatory documents, balancing sponsor queries, and ensuring study cost efficiency. You will also have the potential to mentor fellow CRAs and assist in training. Travel is required for this role. ICON offers competitive salaries, health benefits, retirement plans, and a supportive work environment that encourages high performance and talent development.

Coordinate and manage clinical trial start-up activities, serve as the primary contact for investigators and research coordinators, communicate with sponsors, and lead projects for process improvement in a clinical research organization setting.

The Statistical Programmer II at ICON will create, validate, and generate statistical programs for clinical research projects, ensuring high-quality outcomes and adherence to project timelines. This role requires 3+ years of experience in statistical programming and a Bachelor's degree in a related field.

Seeking and completing clinical trial assignments in an accurate and timely manner, maintaining communication with clinical operations manager, executing recruitment plans, attending investigator meetings, performing technical study requirements, documenting data and adverse reactions, and building relationships with investigators.

The Account Executive is responsible for managing client relationships, providing consultation, managing budgets, and forecasting revenue and activity. This role focuses on business development for Biometrics, Clinical Data, and Medical Writing services.

Client Relationship Manager responsible for implementing large-scale data aggregation and integration projects at Symphony Health. Key client interface and project manager for projects involving patient de-identification process and multiple data sources. Works closely with internal technology and operations teams to deliver customized services to clients.

Senior Statistical Programmer II at ICON plc, responsible for overseeing programming deliverables, leading multiple projects, and providing technical expertise in statistical programming. Requires 8+ years of experience in clinical research industry and expertise in SAS, SDTM, and ADAM programming.

Lead site activation activities for clinical trials, develop plans for country and site distribution, oversee project delivery, ensure compliance with regulations and quality standards, and lead sponsor initiatives. Utilize project management skills to optimize performance and collaboration for successful study outcomes.

ICON Clinical Research is seeking a Senior Account Executive to generate new and repeat business, promote services, and build strong relationships within the Pharmaceutical, Biotechnology, and Medical Device industries. The role involves maximizing success through smooth processes and highlighting ICON's operational strength.

Implement annual sales plan, prospect leads for new RFPs, collaborate with cross-functional teams, update opportunities in Salesforce, represent company at industry events

Coordinate and facilitate activities related to clinical trial start-up requirements and activities for investigational pharmaceutical and biological products. Ensure processes comply with guidelines and regulations for quality and efficiency in a dynamic and supportive environment at ICON.

The CRC Level I (Clinical Research Coordinator) ensures the safety of volunteers, promotes the mission of Accellacare, and coordinates and completes studies according to protocols. This role involves technical and clinical requirements of study protocols, attending investigator meetings, monitoring complications with study drugs, documenting data and adverse reactions, recruiting participants, preparing study documentation, and maintaining clinical supplies.

Lead clinical trial start-up activities by understanding client objectives, developing country and site distribution plans, overseeing site activation, and ensuring study compliance with sponsor timelines and regulations. Utilize project management skills to optimize performance for successful study outcomes.

Elicit and document business requirements, translate them into UML models and technical specifications, create application reports, collaborate with cross-functional teams, and create requirements breakdown structure. Design and build user stories and use cases for review and approval.

Lead cross-functional project planning and implementation, define project scope and tasks, manage project budget and timelines, develop risk mitigation strategies, track deliverables, provide team direction, monitor progress, and evaluate project results. Requires 5 years' medical device experience, 2 years' project management experience, and proficiency in MS Office applications.

Oversee data management strategy and project plans for clinical data collection, lead cross-functional teams, ensure project plan execution, represent global data management, manage clinical trials in compliance with regulations and policies, lead study team meetings, and contribute to process improvement measures.

As a Senior Clinical Research Associate at ICON, you will work within a dynamic and supportive environment, coordinating activities to monitor clinical studies in phases II - IV and ensuring adherence to regulations and ICH-GCP principles. You will be responsible for site selection, initiation, and close-out, as well as maintaining study documentation and assisting in regulatory submissions.

Seeking an Enterprise Account Manager to manage post-sale relationships with platform subscription customers, oversee onboarding and implementation, and represent the voice of the customer in partnership with the product team. Responsible for maximizing customer experience, ensuring product adoption, and supporting renewals and upsells.