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- Tasks: Join us as a Principal Statistician, leading clinical trial data analysis and ensuring top-notch quality.
- Company: Phastar is a global leader in biometric CRO services, known for its commitment to quality and employee satisfaction.
- Benefits: Enjoy flexible working hours, structured training, and a fun, supportive 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 or related field, with experience in the pharmaceutical industry.
- Other info: Remote work available; we value diversity and equal opportunities for all applicants.
The predicted salary is between 43200 - 72000 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 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 datasets
- Program and validate complex summary tables, listings and figures, program statistical analysis tables, according to the SAP
- Liaise with clients to propose alternatives or additional analyses if needed
- Develop and validate macros for statistical analyses and figures
- Perform stage 3 QC
- Advise on complex analyses and endpoints; ensure consistency across clinical trial program
- Create, validate and QC of efficacy dataset specifications for single studies, ISS/ISEs, etc
- Write ISS/ISE SAPs; DSMB SAPs and Charters
- Write project level or therapeutic area level documentation
- Perform QC of SAP text and develop standard SAP text and templates to be used within the company
- Identify the need and provide review of new standards and project level shells ensuring consistency across clinical trial programs
- Write statistical section of protocol for any study
- Provide statistical consultancy at study design stage or during program development
- Conduct independent critical protocol review
- Consult with clinical scientists to decide on best approach for sample size calculation, and execution
- Perform QC of sample size calculations
- Perform complex simulations
- Create complex randomisation schemes and QC of complex randomisation schemes
Qualifications
- Educated to PhD or MSc in Biostatistics, statistics or a 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
- Experience of writing SAPs, protocols
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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Principal Statistician - FSP employer: PHASTAR
Contact Detail:
PHASTAR Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Principal Statistician - FSP
✨Tip Number 1
Familiarize yourself with the specific statistical methodologies and software that are commonly used in clinical trials. Being able to discuss your experience with these tools during an interview can set you apart from other candidates.
✨Tip Number 2
Network with professionals in the pharmaceutical and biotech industries. Attend relevant conferences or webinars where you can meet potential colleagues and learn more about the latest trends in biostatistics.
✨Tip Number 3
Prepare to discuss your previous experiences with Statistical Analysis Plans (SAPs) and how you've contributed to successful clinical trials. Highlighting specific examples will demonstrate your expertise and readiness for the role.
✨Tip Number 4
Show your passion for quality and teamwork during the interview process. Phastar values a collaborative environment, so be ready to share how you've worked effectively in teams and supported your colleagues in past projects.
We think you need these skills to ace Principal Statistician - FSP
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Principal Statistician position. Understand the key responsibilities and qualifications required, such as experience with SAPs and clinical trials.
Tailor Your CV: Customize your CV to highlight relevant experience in biostatistics, programming, and any previous roles in the pharmaceutical industry. Emphasize your familiarity with GCP and regulatory requirements.
Craft a Strong Cover Letter: Write a compelling cover letter that showcases your passion for quality and technical expertise. Mention specific experiences that align with the responsibilities of the role, such as leading statistical analyses or consulting on study designs.
Highlight Teamwork and Leadership Skills: Since the role involves teamwork and potential line management responsibilities, be sure to include examples of how you've successfully collaborated with others and led projects in your previous positions.
How to prepare for a job interview at PHASTAR
✨Understand the Phastar Discipline
Familiarize yourself with Phastar's unique approach to data analysis. Be prepared to discuss how your experience aligns with their commitment to outstanding quality and technical expertise.
✨Showcase Your Statistical Knowledge
Be ready to demonstrate your understanding of biostatistics, particularly in the context of clinical trials. Prepare examples of complex analyses you've conducted and how they contributed to study outcomes.
✨Prepare for Team Collaboration Questions
Since teamwork is emphasized, think of instances where you've successfully collaborated with others. Highlight your willingness to help and support colleagues, especially in a lead statistician role.
✨Discuss Regulatory Awareness
Given the importance of GCP and regulatory requirements, be prepared to discuss your familiarity with these standards. Share experiences where you ensured compliance in your previous roles.
