Principal Statistician

Phastar is a multiple award-winning global biometric Contract Research Organization (CRO) that is accredited as an outstanding company to work for by Best Companies. We partner with pharmaceutical, biotechnology and medical device organizations to provide the expertise and processes to manage and deliver on time, quality biostatistics, programming, data management and data science services. With offices across the UK, US, Germany, Denmark, Kenya, Australia, India, China and Japan, Phastar is the second largest specialized biometrics provider globally, and the largest in the UK.
Our unique approach to data analysis, "The Phastar Discipline", has led us to build a reputation for outstanding quality. With this as our core focus, we're looking for talented individuals who share our passion for quality and technical expertise to join our team.
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, part-time hours, 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 Work as a statistician on clinical trials; producing and validating complex outputs to excellent quality whilst adhering to deliverable timelines. Producing and reviewing Statistical Analysis Plans (SAPs), protocols and other pertinent study documentation. Acting as lead statistician within a reporting team environment, being responsible for statistical aspects of reporting out study results. Working as a global lead statistician across multiple studies, overseeing more junior leads and supporting regulatory interactions. Preparing randomisation schedules and acting as the unblinded statistician on reporting teams. Acting as a statistical consultant to pharmaceutical or biotech companies. Excellent team work ethos, and willingness to help others. Potential to have line management responsibilities.
Responsibilities: Program and validate complex primary efficacy datasetsProgram and validate complex summary tables, listings and figures, program statistical analysis tables, according to the SAPLiaise with clients to propose alternatives or additional analyses if neededDevelop and validate macros for statistical analyses and figuresPerform stage 3 QCAdvise on complex analyses and endpoints; ensure consistency across clinical trial programCreate, validate and QC of efficacy dataset specifications for single studies, ISS/ISEs, etcWrite ISS/ISE SAPs; DSMB SAPs and ChartersWrite project level or therapeutic area level documentationPerform QC of SAP text and develop standard SAP text and templates to be used within the companyIdentify the need and provide review of new standards and project level shells ensuring consistency across clinical trial programsWrite statistical section of protocol for any studyProvide statistical consultancy at study design stage or during program developmentConduct independent critical protocol reviewConsult with clinical scientists to decide on best approach for sample size calculation, and executionPerform QC of sample size calculationsPerform complex simulationsCreate complex randomisation schemes and QC of complex randomisation schemesWork as unblinded DSMB statistician involved with liaising with committee membersDistribute and communicate interim analyses to appropriate stakeholdersAttend meetings as the independent statistician on the DSMB committeeCoordinate and lead clinical interpretation meetingsComplete clinical trial transparency forms and input into project level regulatory documentationSenior review of CSRArchive study documentation following instructions in supplied SOPsPrioritise quality in all activities undertaken, by ensuring the principles in the PHASTAR checklist are followed rigorously, and carefully performing self QC of own workImplement Good Clinical Practice and adhere to regulatory requirements at all timesInitiate projects/ ideas for furthering statistical researchDevelop and deliver company-wide trainingWork as a global lead statistician responsible across multiple studies/ projectsWork as oversight statistician for regulatory submissionsWork independently as a statistical lead on behalf of other companiesCreate, review and update processes and SOPs, identify areas where new processes are requiredQualifications: Educated to PhD or MSc in Biostatistics, statistics or a related disciplineExperience within the pharmaceutical industry to have a good awareness of clinical trial issues, design, and implementation.Familiarity with GCP and regulatory requirementsExperience of writing SAPs, protocolsAPPLY NOW With the world's eyes focused on clinical trial data, this is a fantastic time to join an award-winning specialized biometric CRO that is renowned for its technical expertise, outstanding quality and cutting-edge data science techniques. We offer flexible working, structured training and development plans, continuous learning opportunities, and a competitive salary and benefits package. We're committed to ensuring our employees achieve a healthy work-life balance, within a supportive, fun and friendly working environment.
Should you feel that you have the right skill set and motivations for this position, please apply
Phastar is committed to the principles and practices of equal opportunities and to encouraging the establishment of a diverse workforce. It is our policy to employ individuals on the basis of their suitability for the work to be performed and their potential for development, regardless of age, sex, race, colour, nationality, ethnic or national origin, disability, marital status, pregnancy or maternity, sexual orientation, gender reassignment, religion, or belief. This includes creating a culture that fully reflects our commitment to equal opportunities for all.

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