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.

ICON plc

Browse and apply for open jobs at ICON plc.

project-manager

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

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.

• Ensure client satisfaction by acting as the Client’s main contact regarding ICON Central Laboratories’ services, including setup and day-to-day management of studies.
• Attend and represent ICL at Client meetings.
• Manage studies in accordance with Good Clinical Practice.
• Provide Clients with regular study updates and communicate study progress to Clients and PM Leadership.
• Represent Project Management at internal interdepartmental or interdivisional meetings within ICON.
• Help train more junior PMs and act in an advisory role to less experienced team members.
• Serve as the tactical site supervisor for project manager in the absence of a Team Lead for work related and administrative tasks.
• Take on additional responsibilities to enhance PM Team tools and Practices as defined by Management.

Senior Project Manager, Laboratory

Senior Project Manager overseeing ICON Central Laboratories study setup and client management. Ensuring compliance with Good Clinical Practice and mentoring junior PMs.

clinical-research

• Serves as lead biostatistician for programs of studies, submissions, or on simple to complex individual studies.
• Oversees statistical activities that support ICON’s interactions with clients and regulatory agencies.
• Reviews and approves statistical methods sections of study protocols, statistical analysis plans and statistical input to reports.
• Prepares and approves research proposals and budgets to provide statistical consulting and to conduct statistical analyses for clients.
• Participates in bid defense meetings and makes presentations at marketing meetings with prospective clients.

Principal Biostatistician

Principal Biostatistician managing clinical trials and statistical analyses for ICON plc. Lead biostatistical efforts in drug development across multiple sponsors focusing on Vaccines, Oncology, and Rare Diseases.

• Act as the sponsor's main contact person in all matters regarding our central laboratory services, following up and responding to clinical study specific inquiries from Sponsors, Physicians, CRA and CRO representatives and the ICON Site Services Department.
• Review newly assigned protocols and Amendments.
• Coordinate and manage the completion of the Clinical Laboratory Worksheet (CLW) and communicate information as required to other departments within ICON Laboratories (and ICON Clinical CRO if appropriate).
• Enter protocol parameter information into PACS//ICOLIMS and other systems for new and/or amended protocols.
• Prepare and QC clinical study specific materials.
• Ensure that proper guidelines for communication are set at study start-up and maintained throughout a study by creating and updating the study specific Communication and Escalation Plan.
• Ensure adherence to the protocol specific monitoring plan.
• Maintain clinical study specific study files and ensure that all appropriate documents are properly maintained.
• Ensure that all necessary documents are archived at study closure.
• Provide Sponsors with study management reports.
• Provide client with support on ICOLabs system.
• Inform team leader about study progress.
• Proactively monitor study budget.
• Set the timelines for and monitor the progress of shipment requests for storage samples and verify data.
• Attend and represent ICON at Sponsor Investigator Meetings, Kick-Off Meeting, Bid Defenses or Initiations.
• Develop new tools, train new employees.
• Performs additional relevant responsibilities as requested by management.

Project Manager II – Laboratory

Project Manager II overseeing clinical laboratory services and client satisfaction in clinical trials at ICON plc. Managing projects, ensuring compliance, and facilitating communication with sponsors and internal teams.

software-engineer

• Developing, validating, and maintaining complex statistical programs (SAS, R, or similar) for data manipulation, analysis, and reporting in clinical trials.
• Collaborating with biostatisticians and cross-functional teams to interpret study requirements and ensure the accurate implementation of statistical analyses.
• Preparing and reviewing statistical analysis plans (SAPs), programming specifications, and derived datasets to meet regulatory standards.
• Ensuring data integrity and compliance with industry regulations, including ICH/GCP guidelines, throughout the programming process.
• Mentoring junior programmers and assisting in training team members on programming techniques and best practices.

Statistical Programmer II

Statistical Programmer II role at ICON focusing on statistical program development and execution for clinical trial analysis. Collaborating with diverse teams to ensure data integrity and compliance.

medical-director

• Providing strategic medical leadership and guidance on project teams.
• Offering expert medical and scientific consultation throughout project lifecycles.
• Ensuring compliance with ethical, legal, and regulatory standards in medical and safety monitoring activities.
• Representing the Medical Affairs Department in business development initiatives.

Medical Director – Oncology

Medical Director responsible for strategic medical leadership and guidance on project teams at ICON plc. Collaborating on compliance and providing expert consultation in oncology projects.

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.

ICON plc

About the company

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53 jobs found

Senior Project Manager, Laboratory

ICON plc

Principal Biostatistician

ICON plc

Project Manager II – Laboratory

ICON plc

Statistical Programmer II

ICON plc

Medical Director – Oncology

ICON plc