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- Tasks: Lead statistical analysis and support clinical studies in a dynamic biotech environment.
- Company: Join a small, innovative Radiopharma company making strides in oncology research.
- Benefits: Enjoy a hybrid work model with flexibility and growth opportunities.
- Why this job: Be part of an exciting journey as the first in-house Biostatistician with excellent future prospects.
- Qualifications: Extensive biostatistics experience in pharma/biotech, strong SAS skills, and oncology knowledge required.
- Other info: This role is based in the UK, with one day on-site in Oxford.
The predicted salary is between 54000 - 84000 £ per year.
AL Solutions are partnered with an exciting, small clinical stage Radiopharma organisation that have recently secured their series A funding and looking for a Senior/Principal Biostatistician to be their first in-house employee within the Biometrics team. Our partner are entering a very exciting period with one of their Oncology studies moving into Phase 2, with a further study on track to enter Phase 1. With this upward trajectory, this is a unique opportunity to join the team in the early stages of their development process, with excellent future prospects as they continue to build. This is a hybrid position, with one day required on-site in Oxford, with a requirement for the candidate to be based in the UK.
Responsibilities:
- Perform the role of the Lead Statistician
- Selection and management of Biometric vendors supporting studies
- Provide input into study design
- Produce Statistical Analysis plans
- Support data review in clinical studies (TFL's, CDISC, SDTM, ADaM and data submission packages including Pinnacle21, define.xml etc)
- Involvement in New Drug Application and Market Authorisation Application, contributing to review of clinical study reports
Experience Required:
- Extensive background working in Biostatistics, within a Pharmaceutical/Biotech environment
- Good understanding of SAS Programming and data management concepts and practices
- Previous experience working within Oncology
- Strong experience with clinical study design
- In-depth knowledge and understanding of CDISC
- Vast knowledge of the drug development process
- Previous experience managing budgets and timelines
Please reach out to Jack Kavanagh for more information on this opportunity!
Senior Biostatistician employer: AL Solutions
Contact Detail:
AL Solutions Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Biostatistician
✨Tip Number 1
Network with professionals in the biostatistics and oncology fields. Attend industry conferences or webinars where you can meet potential colleagues and learn more about the latest trends in clinical studies.
✨Tip Number 2
Familiarise yourself with the specific software and tools mentioned in the job description, such as SAS and Pinnacle21. Consider taking online courses or tutorials to enhance your skills and demonstrate your commitment to the role.
✨Tip Number 3
Research the company and its recent developments, especially regarding their oncology studies. Being knowledgeable about their projects will help you engage in meaningful conversations during interviews and show your genuine interest in their work.
✨Tip Number 4
Prepare to discuss your previous experiences managing budgets and timelines in clinical studies. Be ready to provide examples of how you've successfully navigated challenges in these areas, as this will be crucial for the role.
We think you need these skills to ace Senior Biostatistician
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your extensive background in Biostatistics, particularly within a Pharmaceutical or Biotech environment. Emphasise your experience with Oncology studies and any relevant SAS programming skills.
Craft a Compelling Cover Letter: In your cover letter, express your enthusiasm for the role and the company. Discuss how your skills align with the responsibilities listed, such as leading statistical analysis and managing biometric vendors.
Showcase Relevant Experience: When detailing your work history, focus on specific projects where you contributed to clinical study design, data review, and drug development processes. Mention any familiarity with CDISC standards and your experience with New Drug Applications.
Proofread and Edit: Before submitting your application, thoroughly proofread your documents. Check for any grammatical errors or typos, and ensure that all information is clear and concise. A polished application reflects your attention to detail.
How to prepare for a job interview at AL Solutions
✨Showcase Your Biostatistics Expertise
Make sure to highlight your extensive background in biostatistics, especially within the pharmaceutical or biotech environment. Be prepared to discuss specific projects you've worked on, particularly in oncology, and how your contributions made a difference.
✨Demonstrate Your Knowledge of CDISC
Since the role requires in-depth knowledge of CDISC standards, be ready to explain your experience with CDISC, including SDTM and ADaM. You might want to prepare examples of how you've applied these standards in previous roles.
✨Discuss Study Design Contributions
The position involves providing input into study design, so come equipped with examples of how you've contributed to clinical study designs in the past. Discuss any challenges you faced and how you overcame them to ensure successful outcomes.
✨Prepare for Questions on Vendor Management
As you'll be responsible for selecting and managing biometric vendors, think about your previous experiences in vendor management. Be ready to discuss how you approached vendor selection, budget management, and timeline adherence in your past roles.
