Job Description
Ready for your next career move? With continued business growth and a strong pipeline of new projects, Veramed is creating new opportunities for Statistical Programmers to work on innovative studies, expand their skills and advance their careers within a supportive, specialist CRO
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We have multiple exciting opportunities for Principal and Senior level Statistical Programmers skilled in SAS and R, to join us on a permanent basis. We can offer fully remote, hybrid or office-based working, training and a very supportive and quality focused environment.
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The purpose of the role is to provide programming support to the statistics and programming department across a range of projects, clients and therapeutic areas. The Senior or Principal Programmer may also perform a supervisory role (e.g. line management and/or project management).
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Key Responsibilities
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Technical
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• Previous experience with SAS and some R experience/knowledge.
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• Perform review of clinical trial documents including protocols, SAPs, CRFs, CSRs
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• Author, review and approve study TFL shells and dataset specifications
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• Author, validate and document SAS programs for datasets, TFLs and macros, applying good
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programming practice
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• Identify data issues and outliers
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• Complete, review and approve CDISC Validation tool reports
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• Identify data and standards issues and resolve or escalate as appropriate
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• Awareness of emerging standards and associated impact to ongoing and future planned trials
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• Maintain proficiency in SAS and awareness of developments
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• Maintain study master file documents and any other documents that are required to be audit ready
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General
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• Lead internal and client study, project and cross functional team meetings effectively
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• Present study updates internally and at client meetings
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• Share scientific, technical and practical knowledge within the team and with colleagues
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• Perform work in full compliance with applicable internal and client policies, procedures, processes
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and training
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• Build effective collaborative working relationships with internal and client team members
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• Ensure learnings are shared across projects or studies
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• Develop and provide internal technical training where appropriate
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• Lead process improvement initiatives
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Minimum Qualification Requirements
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• BSc, MSc or PhD in numerical discipline (or relevant equivalent industry experience)
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• At least 6 years of relevant industry experience
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Other Information/ Additional Requirements
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• Understanding of clinical drug development process, relevant disease areas, endpoints and study
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designs
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WHAT TO EXPECT:
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- A warm, friendly working environment in which to thrive both personally and professionally.
- A supportive, open-door management policy that will aid in your development and provide you with the tools to take your career to the next level.
- A truly unique CRO that’s doing something different when it comes to managing staff, projects and building relationships in the industry.
- The ability to own your role and develop your skills and experience.
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