Clinical Research Services
Providing clients with a flexible approach to improve cycle times, constrain costs and reduce risks. Specialising in the planning, management, execution, and analysis of Phase II-III clinical trials.
Pressures such as stricter regulations, changing technologies and globalisation are stressing current operational models and information infrastructure to the limits. As these pressures intensify, applying the right methodology to anticipate the challenges that arise during the course of clinical trials is the only way to increase project success.
Other ICON Clinical Research Services include:
- BiostatisticsInnovative clinical trial designs that take advantage of our in depth statistical expertise.
- Data ManagementFast delivery of high quality and meaningful data means that you can make well informed decisions earlier in the trial. This also ensures patient protection and reliable trial results.
- Endpoint Adjudication ServicesEndpoint Adjudication can help to lower the risk of variation in important clinical trial outcome events for submission to regulatory agencies.
- Interactive Response TechnologyInteractive Response Technology systems can effectively solve trial challenges including patient enrolment, randomisation, and dosing.
- Investigator PaymentsTimely and accurate Investigator payments are critical for keeping sites motivated and driving site performance in a study.
- Medical AffairsExperienced physicians and clinical research professionals support the planning, conduct, and evaluation of clinical trials.
- Medical Writing & PublishingMedical and regulatory documentation developed by experienced medical writing teams plays a pivotal role in the success of a clinical research project.
- Pharmacovigilance300+ global pharmacovigilance experts bring together all safety services into a seamless delivery solution.
- Regulatory AffairsSound regulatory strategies critically important in the ever evolving regulatory environment of clinical trials.
Biostatistics
Innovative clinical trial designs that take advantage of our in depth statistical expertise.
Data Management
Fast delivery of high quality and meaningful data means that you can make well informed decisions earlier in the trial. This also ensures patient protection and reliable trial results.
Endpoint Adjudication Services
Endpoint Adjudication can help to lower the risk of variation in important clinical trial outcome events for submission to regulatory agencies.
Interactive Response Technology
Interactive Response Technology systems can effectively solve trial challenges including patient enrolment, randomisation, and dosing.
Investigator Payments
Timely and accurate Investigator payments are critical for keeping sites motivated and driving site performance in a study.
Medical Affairs
Experienced physicians and clinical research professionals support the planning, conduct, and evaluation of clinical trials.
Medical Writing & Publishing
Medical and regulatory documentation developed by experienced medical writing teams plays a pivotal role in the success of a clinical research project.
Pharmacovigilance
300+ global pharmacovigilance experts bring together all safety services into a seamless delivery solution.
Regulatory Affairs
Sound regulatory strategies critically important in the ever evolving regulatory environment of clinical trials.
We are raising the bar in clinical excellence. By focusing on metrics that matter we are already delivering economic value to our clients. Our experience ranges from small studies to large, complex, multinational projects.
COVID-19 clinical operations
Keeping your clinical trial on track in an evolving environment.
Adapting operations to changing conditions
ICON has adapted its services to support sponsors during this time; offering remote monitoring where on-site visits were not permitted, providing additional support to get IMP to patients and pre-recording investigator meetings because of travel restrictions.