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- Tasks: Join us as a Senior Statistician, leading clinical trial data analysis and ensuring top-notch quality.
- Company: Phastar is a globally recognized CRO known for its excellence in biostatistics and data science.
- Benefits: Enjoy flexible working hours, structured training, and a supportive, fun work environment.
- Why this job: Make an impact in clinical trials while helping the planet with our tree-planting initiative.
- Qualifications: PhD or MSc in Biostatistics required; experience in the pharmaceutical industry is a plus.
- Other info: This role is remote-friendly, allowing you to work from anywhere in the UK.
The predicted salary is between 36000 - 60000 ÂŁ per year.
Overview
THE COMPANY
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 Senior 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 a 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 teamwork ethos and willingness to help others.
Responsibilities
Employees may be required to perform some or all of the following:
- Program and validate primary efficacy datasets
- Program and validate summary tables, listings and complex figures, program statistical analysis tables, according to the SAP, given specifications and pertinent study documentation
- Liaise with clients to propose alternatives or additional analyses if needed
- Develop macros for statistical analyses and figures
- Create, validate and QC of efficacy dataset specifications for single studies, ISS/ISEs, etc.
- Write SAP text for any study
- Quality Control of TLF shells
- Lead review process of shells with medical writing and other stakeholders
- Simple clinical study design without supervision
- Manage day-to-day workload to ensure project deliverables are met
- Awareness of CDISC standards
- Consult with clinical scientists to decide on best approach for sample size calculation, and execution
- Perform simple simulations with supervision
- Create actual randomisation schemes and QC of dummy randomisation schemes
- Work as unblinded lead reporting statistician producing unblinded outputs
- Putting together slides for clinical interpretation meetings
- Review of clinical study reports for accuracy
- Archive study documentation following instructions in supplied SOPs
- Prioritise quality in all activities undertaken, by ensuring the principles in the PHASTAR checklist are followed rigorously, and carefully performing self QC of own work
- Implement Good Clinical Practice and adhere to regulatory requirements at all times
- Work in a team for furthering statistical research
- Assist in development of internal training courses
- Act as a Lead Statistician, ensuring quality and timely delivery of statistical aspects of study
- Liaise with Lead Programmer and Study Project Lead regarding resourcing and deliverables
- Responsible for study level resources
Qualifications
· PhD or MSc in Biostatistics or related discipline
· Experience within the pharmaceutical industry to have a good awareness of clinical trial issues, design, and implementation. Familiarity with GCP and regulatory requirements.
APPLY 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, part-time hours, 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! Please note that we are considering candidates located anywhere in the UK as this role can be carried out remotely.
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.
Important notice to Employment businesses/Agencies
Phastar does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Phastar\’s Head of Talent Acquisition to obtain prior written authorization before referring any candidates to Phastar. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and Phastar. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of Phastar. Phastar shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
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Senior/ Principal Statistician employer: PHASTAR
Contact Detail:
PHASTAR Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior/ Principal Statistician
✨Tip Number 1
Familiarize yourself with Phastar's unique approach to data analysis, known as The Phastar Discipline. Understanding their methodology will help you align your skills and experiences with their expectations during interviews.
✨Tip Number 2
Highlight your experience in clinical trials and your familiarity with GCP and regulatory requirements. Be prepared to discuss specific projects where you successfully managed statistical aspects and how you contributed to the quality of deliverables.
✨Tip Number 3
Showcase your teamwork ethos and willingness to support others. Phastar values collaboration, so be ready to provide examples of how you've worked effectively in teams and helped junior colleagues in previous roles.
✨Tip Number 4
Research Phastar's commitment to employee engagement and work-life balance. During your interview, express how these values resonate with you and how you can contribute to maintaining a supportive and friendly work environment.
We think you need these skills to ace Senior/ Principal Statistician
Some tips for your application 🫡
Understand the Role: Take the time to thoroughly read the job description for the Senior Statistician position. Make sure you understand the responsibilities and qualifications required, as this will help you tailor your application effectively.
Highlight Relevant Experience: In your CV and cover letter, emphasize your experience in biostatistics, particularly within clinical trials. Mention specific projects or roles where you produced Statistical Analysis Plans (SAPs) or worked with pharmaceutical companies.
Showcase Your Skills: Clearly outline your technical skills related to statistical programming and data analysis. Include any relevant software or programming languages you are proficient in, as well as your familiarity with GCP and regulatory requirements.
Personalize Your Application: Make your cover letter personal by expressing why you want to work at Phastar specifically. Mention their commitment to quality and employee engagement, and how your values align with theirs.
How to prepare for a job interview at PHASTAR
✨Showcase Your Technical Expertise
As a Senior Statistician, it's crucial to demonstrate your deep understanding of biostatistics and clinical trial methodologies. Be prepared to discuss specific statistical techniques you've used in past projects and how they contributed to successful outcomes.
✨Familiarize Yourself with Phastar's Approach
Research Phastar's unique approach to data analysis, known as The Phastar Discipline. Understanding their commitment to quality and how it aligns with your own values will help you articulate why you're a great fit for the team.
✨Prepare for Teamwork Scenarios
Given the emphasis on teamwork in the role, think of examples from your past experiences where you successfully collaborated with others. Highlight your ability to lead and support junior statisticians, as well as your willingness to help colleagues.
✨Discuss Regulatory Knowledge
Since familiarity with GCP and regulatory requirements is essential, be ready to discuss your experience with these standards. Share specific instances where your knowledge positively impacted a project or helped navigate challenges in clinical trials.
