Project Description
Principal Statistician
Based in either RTP (NC, US), London, Macclesfield, Kent, Glasgow (UK) or Newcastle (Australia)
- Ability to lead a team of statisticians and programmers to manipulate, summarise and analyse clinical trial data using a variety of statistical methods, ultimately delivering clinical trial results to an agreed timeline with optimal quality
- Project management responsibilities, including allocating staff, predicting and planning resources
- Preparation and review of study documentation e.g. protocols and statistical analysis plans
- Ability to advise, mentor and teach both internal and external statisticians with regards to statistical and data analysis methods
- Function as a study expert across a number of studies, helping to clarify details on analysis methods for the internal PHASTAR team
- Responsible for ensuring the team meets the highest quality standards, and follows the principles detailed in PHASTAR’s internal procedures
- Maintaining a positive and engaging client relationship with regards to statistical issues
Candidate Requirements
- PhD or MSc in Biostatistics or related 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
- Ability to communicate with a broad range of people across different functions
Senior Statistician
Based in either RTP (NC, US), London, Macclesfield, Kent, Glasgow (UK) or Newcastle (Australia)
- Manipulate, summarise and analyse clinical trial data using a variety of statistical methods
- Function as statistical support across a number of studies
- Preparation of study protocols and development of statistical analysis plans
- Ability to communicate Statistical issues across multi-disciplinary team
- Supervise work of less experienced Statisticians
- Being a client contact for the Biostatistics team
Candidate Requirements
- PhD or MSc in Biostatistics or related discipline
- Experience working within a clinical trials environment (Pharma, CRO or academia)
- Previous experience working with SAS
- Excellent written and verbal communication
- Familiarity with GCP and ICH guidelines
Principal Statistical Programmer
Based in either RTP (NC, US), London, Macclesfield, Kent, Glasgow (UK) or Newcastle (Australia)
- 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
- 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
Senior Statistical Programmer
Based in either RTP (NC, US), London, Macclesfield, Kent, Glasgow (UK) or Newcastle (Australia)
- 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 (CRF) to CDISC standards
- Feeding back data errors to client data management teams
- Attendance to regular client meetings to provide updates on projects and timelines
- Assist internal management team in assessing resourcing needs for successful completion of assigned projects
- Working towards industry (CDISC) and client standards
Candidate Requirements:
- BSc, MSc or PhD in Mathematics, Science or IT related discipline
- Previous experience working within a clinical trials environment (Pharma or CRO)
- Previous experience working with SAS
- CDISC experience, specifically SDTM and AdaM is highly desired but not essential
- Previous experience in leading teams highly beneficial but not essential
- Excellent written and verbal communication
For all the above positions, we can 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) - Excellent remuneration (competitive salary, pension, healthcare, conferences and courses etc)