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| Job Location | London |
| Education | Not Mentioned |
| Salary | Salary negotiable |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Contract, full-time |
A remote 1 year contract for a Senior Statistician is available to be responsible for leading all statistical activities relating to clinical trial projects. Provision of statistical consultancy in support of clients.Responsibility :Performing the Lead Statistician role for assigned projects with successful deliveries to planned timelines, budget and qualityDevelopment and validation of statistical analyses in SASPreparation and review of statistical analysis plans and specifications.Providing statistical expert point of contact with sponsor and internal project teamsRandomisations, protocol and sample size consultancyPeer review of statistical deliverablesProviding statistical expertise and presentation of results at sponsor meetingsProviding statistical evaluation and reports for inclusion into Clinical Study ReportsAdherence to GCP and relevant regulatory documents; design of studies to relevant standards and guidelines.General responsibilities include:Providing expert advice on statistical issues, contributing to the expansion of the departments knowledge baseContributing to the company development of new systems, processes and SOPsBusiness development expert support - contributing to proposals, contracts and meetingsExperience and skills required:Strong analytical and data interpretation skillsStatistical expertise in a variety of therapeutic areasStatistical programming and modelling with current experience across a variety of statistical topicsAbility to communicate well verbally and in writing with people at different levels across the organisation and with different levels of statistical understandingWorked on multiple studies as a lead statisticianMinimum of 3 years in the Pharmaceutical or CRO industriesProject management, organisational and matrix management skills with the ability to proactively prioritise projectsExperience with performing statistical analysis using SAS v. 9Experience and understanding of CDISCClinical development knowledge across Phase I through IV studies and real world studies Required skills
Keyskills :
Statistics CRO Programmer CDISC