Senior Biostatistician I

Senior Biostatistician I

Manchester Full-Time 36000 - 60000 £ / year (est.) Home office possible
Go Premium
M

At a Glance

  • Tasks: Lead statistical planning and analysis for clinical trials while programming with SAS/R.
  • Company: Join a dynamic CRO focused on innovative clinical trial solutions.
  • Benefits: Remote work, competitive salary, and opportunities for professional growth.
  • Why this job: Make a real impact in clinical research while honing your biostatistics and programming skills.
  • Qualifications: Experience in biostatistics and strong programming skills in SAS/R required.
  • Other info: Collaborative environment with a focus on quality and regulatory compliance.

The predicted salary is between 36000 - 60000 £ per year.

Job Title: Senior Biostatistician I – (with Programming Support)

Location: (Remote – United Kingdom)

About the Role:

We are seeking a Senior Biostatistician to join an embedded team in a CRO. This role is primarily focused on biostatistical design, analysis, and reporting for clinical trials, while also requiring hands-on programming support (SAS/R) as the team integrates both functions.

You will play a key role in ensuring the statistical integrity and quality of clinical trial deliverables, working closely with cross-functional teams including programmers, data managers, and project managers. This is an ideal role for someone who wants to remain hands-on with biostatistics while also contributing to programming and reporting tasks.

Key Responsibilities:

  • Lead statistical planning and analysis for clinical trials, including efficacy, safety, and exploratory endpoints.
  • Develop and implement statistical analysis plans (SAPs) and contribute to study design discussions, including sample size calculations, randomization, and stratification strategies.
  • Program and validate statistical outputs using SAS or R, including tables, listings, and figures (TLFs) for study reports and regulatory submissions.
  • Ensure all statistical and programming deliverables comply with regulatory standards (ICH-GCP, FDA/EMA guidelines) and internal quality requirements.
  • Collaborate closely with other biostatisticians and programmers within the same team to ensure consistent and high-quality study deliverables.
  • Act as the primary statistical resource for assigned studies while providing support for programming tasks as needed.
  • Support client engagement, providing statistical input and guidance on study deliverables, while reporting internally for professional development and support.

Requirements:

  • Proven experience as a biostatistician in clinical trials, ideally at Senior I / early Senior II level.
  • Strong programming skills in SAS and/or R, with the ability to produce and validate outputs independently.
  • In-depth knowledge of clinical trial design, statistical methodology, and regulatory requirements.
  • Experience in FSP or embedded client roles is advantageous.
  • Self-motivated, detail-oriented, and comfortable working both independently and as part of a cross-functional, integrated statistics/programming team.

eireann.evans@meetlifesciences.com

Senior Biostatistician I employer: Meet Life Sciences

Join a forward-thinking CRO that values innovation and collaboration, offering a remote work environment in the United Kingdom. As a Senior Biostatistician I, you will benefit from a supportive culture that prioritises professional growth, with opportunities to enhance your skills in both biostatistics and programming. Enjoy the flexibility of remote work while being part of a dynamic team dedicated to delivering high-quality clinical trial results.
M

Contact Detail:

Meet Life Sciences Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior Biostatistician I

✨Tip Number 1

Network like a pro! Reach out to your connections in the biostatistics field, attend relevant webinars, and join online forums. You never know who might have the inside scoop on job openings or can refer you directly.

✨Tip Number 2

Prepare for interviews by brushing up on your SAS and R skills. Be ready to discuss your past projects and how you've tackled statistical challenges. Practising common interview questions can also help you feel more confident.

✨Tip Number 3

Showcase your hands-on experience! When chatting with potential employers, highlight specific examples of your work in clinical trials, especially any programming tasks you've handled. This will demonstrate your dual expertise.

✨Tip Number 4

Don't forget to apply through our website! We love seeing candidates who are genuinely interested in joining our team. Plus, it gives you a chance to showcase your enthusiasm for the role right from the start.

We think you need these skills to ace Senior Biostatistician I

Biostatistical Design
Statistical Analysis
SAS Programming
R Programming
Statistical Analysis Plans (SAPs)
Sample Size Calculations
Randomization Strategies
Stratification Strategies
Regulatory Compliance (ICH-GCP, FDA/EMA)
Clinical Trial Methodology
Cross-Functional Collaboration
Detail-Oriented
Self-Motivated
Client Engagement

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in biostatistics and programming. We want to see how your skills align with the role, so don’t be shy about showcasing relevant projects or achievements!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about biostatistics and how you can contribute to our team. We love hearing personal stories that connect you to the role.

Showcase Your Programming Skills: Since this role involves hands-on programming support, make sure to mention your proficiency in SAS and R. We’re keen to know how you’ve used these tools in past projects, so give us the details!

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy!

How to prepare for a job interview at Meet Life Sciences

✨Know Your Stats

Brush up on your biostatistical knowledge and be ready to discuss specific methodologies you've used in past clinical trials. Be prepared to explain how you approach statistical planning and analysis, especially regarding efficacy and safety endpoints.

✨Show Off Your Programming Skills

Since programming support is a key part of the role, make sure you can demonstrate your proficiency in SAS or R. Bring examples of statistical outputs you've programmed and validated, and be ready to discuss any challenges you faced and how you overcame them.

✨Understand Regulatory Standards

Familiarise yourself with ICH-GCP, FDA, and EMA guidelines. During the interview, highlight your experience ensuring compliance with these standards in your previous roles, as this will show that you understand the importance of regulatory requirements in clinical trials.

✨Collaborate and Communicate

Emphasise your ability to work within cross-functional teams. Share examples of how you've collaborated with programmers, data managers, and project managers to deliver high-quality study outputs. Good communication skills are essential, so be ready to discuss how you engage with clients and provide statistical guidance.

Senior Biostatistician I
Meet Life Sciences
Go Premium

Land your dream job quicker with Premium

You’re marked as a top applicant with our partner companies
Individual CV and cover letter feedback including tailoring to specific job roles
Be among the first applications for new jobs with our AI application
1:1 support and career advice from our career coaches
Go Premium

Money-back if you don't land a job in 6-months

M
  • Senior Biostatistician I

    Manchester
    Full-Time
    36000 - 60000 £ / year (est.)

    Application deadline: 2027-10-10

  • M

    Meet Life Sciences

Similar positions in other companies
UK’s top job board for Gen Z
discover-jobs-cta
Discover now
>