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Senior Statistical Programmer
3 months ago
Overview
ABOUT PHASTAR PHASTAR is a multiple award-winning global biometrics Contract Research Organisation (CRO). We partner with pharmaceutical, biotechnology and medical device organisations to provide the expertise and processes to manage and deliver on time, quality biostatistics, programming, data management and data science services. Operating across the UK, US, Canada, France, Spain, Germany, Kenya, Australia, India, China, and Japan, PHASTAR is the second largest specialised biometrics provider globally, and the largest in the UK. WHY PHASTAR Accredited as an outstanding company to work for, PHASTAR is committed to employee engagement, workplace satisfaction and ensuring a healthy work-life balance. We offer flexible working, involvement in developing company-wide initiatives, structured training and development plans, and a truly supportive, fun, and friendly environment. What's more, when you join our team, PHASTAR will plant a tree in your honour, as one of our Environmental, Social and Governance (ESG) initiatives. So, not only would you get your dream job, you'll also be helping to save the planet THE ROLE Demand for our Functional Service Provision is growing, and we're looking for talented individuals who share our passion for quality and technical expertise to join our FSP team. All positions can be remote. As a senior/principal statistical programmer working within FSP, you will be fully integrated into our sponsor's team as a key contributor, providing that partner with hands-on technical expertise and project oversight. Our FSP positions provide the unique opportunity to work for a growing CRO that is recognised for its continuous learning and development opportunities, whilst also gaining direct experience of working within a sponsor's pharmaceutical environment.Responsibilities
- Project leadership of assigned studies
- Assign tasks to team members and provide oversight of their work
- Work cross-functionally with other clinical team members
- Negotiate timelines and scope of work
- Work and make decisions independently
- Manipulation of data to produce analysis datasets, including SDTM and ADaM datasets
- Production and review of Tables, Figures and Listings (TFLs) according to statistical analysis plans
- Creation and review of programming specifications and, if required, annotation of case report forms (CRFs) to CDISC standards
- Attendance at regular client meetings to provide updates on projects and timelines
- Assisting internal management team in assessing resourcing needs for successful completion of assigned projects
- Working to industry (CDISC) and client standards
- Bsc, MSc or PhD in mathematics, science or IT related discipline
- Experience working within a clinical trials environment
- Substantial experience working with SAS
- CDISC (SDTM and ADaM) experience
- Previous experience of leading teams is preferred but not essential
- Excellent written and verbal communication skills
