Overview
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, Germany, Spain, 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!
Responsibilities
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 statistician 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.
- Work as global lead statistician across multiple clinical studies; managing resources, timelines, and quality
- Assign tasks to team members and provide oversight of their work
- Act as a statistical consultant to pharmaceutical/biotechnology sponsors
- Work cross-functionally with other clinical team members
- Negotiate timelines and scope of work
- Work and make decisions independently
- Write statistical section of protocol for simple study design
- Produce and review Statistical Analysis Plans (SAPs), protocols, and other study documentation
- Prepare randomisation schedules and act as the unblinded statistician on reporting teams
- Program and validate summary tables, listings, and complex figures, and program statistical analysis tables
- Develop and validate macros for statistical analyses and figures
- Create, validate and QC efficacy dataset specifications for single studies, ISS/ISEs
- Work to industry (CDISC) and client standards
Qualifications
- MSc or PhD in biostatistics or related discipline
- Experience working as a statistician within a clinical trials environment
- SAS programming skills
- CDISC (SDTM and ADaM) experience
- Project leadership skills
- Excellent written and verbal communication skills
APPLY NOW
With the world’s eyes focused on clinical trial data, this is a fantastic time to join an award-winning specialised biometrics CRO that is renowned for its technical expertise, outstanding quality, and cutting-edge data science techniques.
*PHASTAR does not accept any CVs received from recruitment agencies. In the event that speculative CVs are submitted by recruitment agencies, PHASTAR reserves the right to contact these candidates directly and consider them for current/future vacancies without any financial obligation to the recruitment agency in question. This applies to any CVs sent directly to any PHASTAR employee.
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