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Coordinate, develop, negotiate, and execute client/sponsor contracts and change orders. Provide QC review of contracts to ensure accuracy. Lead discussions and negotiations with legal and sales teams. Embrace process improvement culture.
The Global Feasibility Manager at ICON plc is responsible for managing and leading the process of clinical Feasibility strategy planning to support pre-award proposals and bid defense processes. They analyze data and leverage analytics tools to define optimal country/site/patient delivery strategies, maintain communication between relevant parties, and mentor less senior associates during bid defense meetings. This role requires expertise in evidence-based feasibility, preparation of Feasibility strategy text, and support for project teams as a technical Feasibility expert.
Seeking a Contract Analyst to review and analyze contracts, negotiate terms, collaborate with teams, maintain records, and provide guidance on contract matters in the clinical research industry.
As a Senior Statistical Programmer I at ICON, you will be responsible for statistical aspects of clinical and preclinical research projects. This includes designing SAS programs, supporting statisticians, and assisting in data management. You should have a Bachelor's or Master's degree in statistics or a related field, with at least 6 years of SAS Programming experience in the Pharmaceutical/CRO industry.
Assisting in identifying study sites, essential document collection, setting up site-related data in clinical systems, acting as primary site contact, ensuring timely data entry, performing risk assessment, adherence to guidelines and regulations.
As a Group Lead/Line Manager in TMF Operations, responsible for managing central filing staff, ensuring activities are performed as per process standards, meeting client needs, and leading the team in achieving productivity and quality targets. Represent TMF Operations during audits and manage findings. Foster a culture of process improvement and mentor team members to drive innovation and excellence in clinical research.
As a Senior Biostatistician I, you will lead biostatistical efforts for clinical studies, develop statistical analysis plans, perform complex analyses, and collaborate with multidisciplinary teams to interpret medical data and advance innovative therapies.
Lead and execute programming deliverables on multiple projects, manage programming team deliverables, develop technical solutions, foster client relationships, and ensure high-quality deliverables in statistical programming.
As a Senior Statistical Programmer, you will lead and execute programming projects while ensuring high-quality deliverables for statistical analysis. You'll develop, validate, and document datasets and analysis outputs, and collaborate closely with biostatistics teams and clients. Strong knowledge of SAS and statistical concepts is essential, alongside experience with regulatory standards and programming procedures.
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