At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives. Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That's our vision. We're driven by it. And we need talented people who share it. If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.
Senior Principal, Patient Centred OutcomesICON Patient Centred Outcomes (PCO) is part of ICON plc, a leading global Clinical Research Organization headquartered in Dublin, Ireland. Our PCO group undertakes consultancy projects for international clients in both the pharmaceutical and medical device sectors, supporting development of medicines and clinical trials. The work of the PCO group focuses on patient-centred research, including health-related quality of life, disease signs and symptoms, treatment preference, adherence and satisfaction. The group is respected globally for the quality and innovation of their applied qualitative and quantitative work. Much of their work involves Clinical Outcome Assessment (COA) measurement development and validation including conducting patient interviews and focus groups, qualitative analysis, and psychometric evaluation.
The candidate will be required to support the PCO practice lead in taking senior managerial responsibility for the department. In addition, the candidate recruited for this role will be expected to utilise their skills in outcomes research and related work to contribute to all aspects of the department's work as well as supporting the development of the team globally.
Key ResponsibilitiesAct as a scientific thought partner with the client and the project team throughout the project.Identify and apply leading edge tools/techniques and develop new and insightful analytic approaches.Develop endpoint reviews that include consolidating evidence, identifying gaps, and proposals on how to address gaps.Critically evaluate COA instruments to identify gaps and strategies to address gaps.Review and finalize project deliverables and ensure study findings are valid and reliable and presented in a manner that is up to a high standard.Lead regulatory EMA/FDA dossier development.Independently develop project plans and scientific content in proposals and achieve good conversion rate of submitted and won proposals.Serve as KOL on project methodology, project risk and project execution.
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