At a Glance
- Tasks: Support statistical programming for clinical trials and collaborate with cross-functional teams.
- Company: Global pharmaceutical organisation focused on innovative clinical development.
- Benefits: 12-month contract with competitive pay and opportunities for professional growth.
- Other info: Join a dynamic team with a focus on quality and regulatory compliance.
- Why this job: Make a real impact in clinical research while working with cutting-edge statistical tools.
- Qualifications: Strong SAS programming skills and experience in clinical research required.
The predicted salary is between 45000 - 60000 € per year.
We are supporting a global pharmaceutical organisation in the search for an experienced Statistical Programmer to join a specialist biometrics function on a contract basis for 12 months initially. This role will focus on supporting independent statistical and safety analysis activities across clinical development programmes, working closely with statisticians and cross-functional study teams.
Key Responsibilities
- Deliver statistical programming support for clinical trial analysis and reporting activities
- Develop and validate datasets, tables, listings, and figures (TLFs)
- Support independent safety and statistical analysis workstreams
- Collaborate with biostatistics and clinical teams to ensure high-quality deliverables
- Contribute to programming standards, QC processes, and regulatory compliance activities
Required Experience
- Strong hands-on experience with SAS programming
- Experience using R within a clinical research or pharmaceutical environment
- Background in statistics, biostatistics, or statistical programming
- Experience supporting clinical trial analysis within biotech/pharma/CRO settings
- Understanding of clinical data standards and reporting requirements
Desirable Experience
- Experience supporting safety analyses or independent statistical review activities
- Familiarity with regulatory submission environments
- Previous experience working within global clinical development teams
Contract Statistical R and SAS Programmer in Twickenham employer: Warman O'Brien
Join a leading global pharmaceutical organisation that values innovation and excellence in clinical development. As a Contract Statistical R and SAS Programmer, you will be part of a collaborative work culture that prioritises professional growth and offers opportunities to contribute to impactful projects in the healthcare sector. With a focus on quality deliverables and regulatory compliance, this role provides a unique chance to enhance your skills while working alongside industry experts in a dynamic environment.
StudySmarter Expert Advice🤫
We think this is how you could land Contract Statistical R and SAS Programmer in Twickenham
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical and clinical research sectors. Attend industry events or webinars to meet potential employers and showcase your skills.
✨Tip Number 2
Prepare for interviews by brushing up on your SAS and R programming skills. Be ready to discuss specific projects you've worked on, especially those involving statistical analysis and clinical trials.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your career goals. Use our website to find roles that match your expertise in statistical programming and clinical development.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can set you apart from other candidates. It shows your enthusiasm for the role and keeps you fresh in their minds.
We think you need these skills to ace Contract Statistical R and SAS Programmer in Twickenham
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your experience with SAS and R, especially in clinical settings. We want to see how your background aligns 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 statistical programming and how your skills can contribute to our team. Keep it concise but impactful – we love a good story!
Showcase Your Collaboration Skills:Since this role involves working closely with statisticians and cross-functional teams, highlight any past experiences where you’ve successfully collaborated. We value teamwork, so let us know how you’ve contributed to group success!
Apply Through Our Website:We encourage you to apply directly through our website for a smoother process. It helps us keep track of applications better and ensures you don’t miss out on any important updates from us!
How to prepare for a job interview at Warman O'Brien
✨Know Your SAS and R Inside Out
Make sure you brush up on your SAS and R programming skills before the interview. Be prepared to discuss specific projects where you've used these tools, as well as any challenges you faced and how you overcame them.
✨Understand Clinical Trial Processes
Familiarise yourself with the clinical trial process and the role of statistical programming within it. Being able to speak knowledgeably about how your work supports clinical development will impress the interviewers.
✨Prepare for Technical Questions
Expect technical questions related to statistical analysis and programming standards. Practise explaining complex concepts in simple terms, as you may need to collaborate with non-technical team members.
✨Showcase Your Teamwork Skills
Collaboration is key in this role, so be ready to share examples of how you've worked effectively within cross-functional teams. Highlight your communication skills and how you ensure high-quality deliverables.
