Job Opening at Phastar

Job description

There is a number of reasons you may wish to join the PHASTAR team:

• Learn from PHASTAR's internal experts and from personnel with specialist PhDs
• A better way to work: PHASTAR have a unique approach to statistical consulting and data analysis. Our approach ensures high quality consulting and data analysis
• A relaxed place to work. PHASTAR encourages a hard working but friendly and sociable office environment

Duties:

We are looking for an experienced programmer who will support programming activities related to the analysis and reporting of data from clinical trials:

• Responsibility for overall project delivery, including clinical trial reports and other regulatory submission deliverables
• Project management responsibilities, including allocating staff, predicting and planning resources
• Act as a study expert for a number of studies, with an ability to clarify details on analysis methods for the internal PHASTAR team
• Advise on internal, client and CDISC data standards
• Manipulation of data to produce/oversee analysis datasets, including SDTM and ADaM datasets
• Production and/oversee the production of Tables, Figures and Listings (TFLs) according to statistical analysis plans
• Responsible for ensuring the team meets the highest quality standards, and follows the principles detailed in PHASTAR’s internal procedures
• Function as a programming expert across a number of studies
• Maintaining a positive and engaging client relationship with regards to statistical and/or programming issues
• Report on study progress to the PHASTAR management team

Candidate Requirements:

• Educated to degree level or equivalent within a relevant discipline.
• Experience working within a clinical trials environment (Pharma, CRO or academic)
• Previous experience performing statistical analysis using SAS
• Excellent written and verbal communication skills
• Experience of working to CDISC standards in both SDTM and ADaM

What we offer:

• Advancement of your career in an intellectually-stimulating, dynamic, supportive environment
• Variety of projects in statistical consultancy and clinical trial reporting (range of therapeutic areas and phases)
• Opportunities to get involved in the management of other statistical and programming staff members