At a Glance
- Tasks: Lead statistical activities in global clinical trials and ensure quality deliverables.
- Company: Aixial Group, a leading International Contract Research Organization.
- Benefits: Competitive salary, mentoring, training, and a supportive team environment.
- Other info: Home-based options available in Romania, Portugal, Spain, or the UK.
- Why this job: Join an innovative team making a real impact in clinical research.
- Qualifications: Masters in Medical Statistics or equivalent, with 5 years CRO experience.
The predicted salary is between 50000 - 70000 £ per year.
The Aixial Group is an International Contract Research Organization (CRO), a member of the ALTEN Group, with offices located in France, UK, US, Belgium, Denmark, Sweden, Switzerland, Romania, and India. The CRO occupies a unique position in the clinical research industry, supporting biotech in clinical trials across all phases (Ph. I - IV) and non-interventional studies, as an expert in the operational delivery of clinical trials. Our vision is to conduct clinical trials better than anyone else, to help patients and ultimately save lives. We have earned a strong reputation for successfully delivering complex, demanding and innovative clinical trials, with specialist therapeutic expertise in oncology, cell & gene therapy, radiopharmaceuticals and rare diseases.
We are currently looking for an enthusiastic and talented Senior Biostatistician willing to be involved in all spectrum of activities, including acting as Lead on studies. This role can be home-based in Romania, Portugal, Spain, or the UK.
Your core responsibilities:
- To provide expert statistical input to Phase I-IV global clinical trials, including the design of clinical trials (protocol, sample size, randomisation, etc) and the production and review of analysis and reporting deliverables (including statistical analysis plans) on behalf of and/or in conjunction with Aixial Group clients.
- Creation and QC of study specifications for ADaM datasets, and statistical programming and QC of ADaM datasets for global Phase I-IV trials.
- Statistical programming and QC of tables, listings and figures for global Phase I-IV trials.
- Responsible for the quality and timeliness of statistical deliverables.
- As lead Statistician, to be primarily responsible for all statistical activities on allocated studies including planning and coordination of activities for assigned statistical team members.
This position is perfect for you if you have:
- Minimum of a Masters (M.Sc.) or equivalent in Medical Statistics or minimum of a degree (or equivalent) in Statistics/Mathematics.
- Minimum of 5 years of experience working for a CRO (including 1 to 2 years leading studies).
- Fluent in spoken and written English.
- Excellent SAS programming skills.
- Experience of project managing (timelines and/or budgets) of statistical activities.
- The ability to perform all duties as a project team member with no supervision.
- The ability to perform all duties of lead team member on several concurrent studies with minimal supervision.
- Computer literacy, ideally in one or more computing systems/programming languages/software packages in addition to SAS.
- Strong oral and written communication skills (including the ability to communicate statistical concepts and information to non-statisticians).
- Good understanding of medical terminology, clinical trial methodology, drug development process and ICH/GCP (especially relating to statistical methodology).
- Good knowledge of statistical principles underlying clinical trials.
- Good awareness of, and familiarity with CDISC requirements.
- Expert knowledge of clinical trial practices, procedures and methodologies.
- Excellent organizational/time management skills.
- Knowledge in developing statistical section of the study protocol and calculating sample size.
- Experience with Bayesian statistics (BOIN, CRM) is a plus.
What we offer:
- Opportunity to be part of an innovative organization and work with exciting technologies.
- Mentoring and training to develop your skills in the clinical trials industry.
- The chance to be part of an effective, friendly, and supportive team.
- Competitive employment package.
For more information on Aixial Group recruitment and consideration for other opportunities, please review the recruitment statement on our careers page - https://www.aixialgroup.com/join-us/
Please be aware that we do not accept resumes from outside agencies or recruiters unless specifically requested by Aixial Group CRO Talent Acquisition. Unsolicited agency or recruiter resumes will not be eligible for referral fees and will be considered candidates Aixial may directly contact for employment application.
Senior Biostatistician - UK/EU (CP07Ti617) in Horsham employer: Aixial Group
Contact Detail:
Aixial Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Biostatistician - UK/EU (CP07Ti617) in Horsham
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and engage with professionals on platforms like LinkedIn. We all know that sometimes it's not just what you know, but who you know that can land you that dream job.
✨Tip Number 2
Prepare for interviews by researching the company and its projects. Understand their values and how they align with your skills as a Senior Biostatistician. We want you to shine in those interviews, so practice common questions and have your own ready to show your interest!
✨Tip Number 3
Showcase your expertise! Bring along examples of your previous work or case studies that highlight your statistical prowess and project management skills. We believe that demonstrating your experience can set you apart from other candidates.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows your enthusiasm for joining our innovative team at Aixial Group. Let’s get you on board!
We think you need these skills to ace Senior Biostatistician - UK/EU (CP07Ti617) in Horsham
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Biostatistician role. Highlight your relevant experience in clinical trials, especially any leadership roles you've had. We want to see how your skills match what we're looking for!
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 mission at Aixial Group. Keep it concise but impactful.
Showcase Your Skills: Don’t forget to highlight your SAS programming skills and any experience with statistical methodologies. We’re keen on seeing how you can bring your expertise to our team, so make it clear!
Apply Through Our Website: We encourage you to apply directly through our careers page. It’s the best way for us to receive your application and ensures you’re considered for this exciting opportunity. Let’s get started!
How to prepare for a job interview at Aixial Group
✨Know Your Stats
Brush up on your statistical knowledge, especially around clinical trials. Be ready to discuss your experience with SAS programming and how you've applied statistical principles in real-world scenarios.
✨Showcase Leadership Skills
As a Senior Biostatistician, you'll likely lead studies. Prepare examples of how you've successfully managed projects or teams in the past, highlighting your ability to coordinate activities and ensure quality deliverables.
✨Understand the Company’s Vision
Familiarise yourself with Aixial Group's mission and values. Be prepared to discuss how your skills and experiences align with their goal of conducting clinical trials better than anyone else and ultimately saving lives.
✨Communicate Clearly
Practice explaining complex statistical concepts in simple terms. You'll need to communicate effectively with non-statisticians, so think of examples where you've successfully done this in previous roles.