SENIOR STATISTICIAN.

Position Purpose

Contract: Permanent full-time/flexible working available (including part-time/compressed hours/term-time working) Location: Belfast office, home-based or hybrid working available Salary: Competitive Salary (based on experience) + attractive benefit package including 37 days holiday, private health insurance, company pension scheme (5% employer) Why you should apply? Have you experience in the application of statistics in the pharmaceutical, healthcare or life science sectors? Do you want to be at the forefront of statistical innovations, leading the way on clinical trial design and analysis? Are you looking for an opportunity that offers you a flexible work solution and one that will take your career to the next level of responsibility? Would you like to join a dynamic, growing firm where you can really make an impact, not just on the company but to accelerate drug development and ultimately benefit patients? We are looking for passionate and motivated statisticians to work within our Services team to deliver high quality, innovative, analytical services within a clinical setting as our KerusCloud platform moves into the next phase. We offer a competitive salary with extensive benefits including generous holiday entitlement (37 days), pension scheme and private health insurance. We provide a fantastic opportunity for professional development both through formal training and through exposure to a variety of challenges with the chance to learn and develop new skills. Key duties Creates and reviews statistical documents such as study protocol, Statistical Analysis Plans (SAPs) and Statistical Analysis Reports (SARs). Performs analyses independently for smaller projects, or as part of a team for larger/complex projects Applies a range of skills and can adapt them to suit many situations, using their discretion to select the most appropriate techniques May act as an internal expert for some skill areas and contribute to the development of internal resources. Delivers results to an agreed timeline with optimal quality. Interacts with a range of stakeholders, communicating proactively. The essentials Degree in mathematics, statistics, physics, pharmacology or with a strong statistical component Typically would have a minimum of 3 years’ relevant experience in the application of statistics on clinical trials (pharma, CRO, academic) Ability to communicate clearly in both written and spoken English Experience in SAS statistical software package Experience in study design and protocol contribution Any of the following would be desirable Higher degree in statistics or similar scientific discipline Experience in statistical software package R Experience of modelling and simulation techniques to explore complex study designs Experience of early-phase drug development processes including innovative/adaptive study design Experience providing recommendations for innovative analysis options to address strategic objectives in discussion with customers Experience in delivering customer projects to high quality standards Please note the successful applicant will be asked for proof of the right to work in the UK.

Job Responsibilities

Requirements