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- Tasks: Lead and execute programming activities for complex clinical trials with top pharmaceutical companies.
- Company: Join a global leader in clinical research with a focus on innovation.
- Benefits: Flexible work options, competitive salary, and opportunities for professional growth.
- Why this job: Make a real impact in healthcare by supporting groundbreaking clinical studies.
- Qualifications: Bachelor’s degree and 1-2 years of SAS programming experience required.
- Other info: 100% remote work available, fostering a dynamic and supportive environment.
The predicted salary is between 36000 - 60000 £ per year.
Overview
As a Statistical Programmer II in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex clinical trials (phases I-III) for renowned, innovative and global top pharmaceutical companies. Oftentimes you will have the opportunity to lead studies through various phases of the clinical development plan and support submissions, regulatory questions, publications as well as ad hoc and post hoc requests.
You can be 100% home-based or if you prefer, you can work from our local office in your home country.
Responsibilities
- With sufficient experience assume the role of a Lead Statistical Programmer for CP studies only with support from senior programming staff.
- Plan, execute and oversee all programming activities on a study, including but not limited to, resource estimation, working within budget, meeting timelines, maximizing quality, interaction with other departments and the client, etc.
- Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs, and perform QC of SDTM, ADaMs and TFLs.
- Produce Define XML/PDFs, Analysis Results Metadata (ARM), annotated eCRFs and Reviews Guides to support SDTMs and ADaMs.
- With support from senior programming staff, develop specifications for SDTMs and ADaM datasets.
- Review SAPs and TFL shells from a programming perspective for studies with support from senior programming staff.
- Respond to QA and client audits with support from senior programming staff.
- And all other duties as needed or assigned.
Qualifications
- Minimum Bachelor’s degree, preferably in mathematics, statistics, computing, life science, health science, or related subjects.
- Typically, 1 – 2 years of SAS programming experience in the CRO or Pharmaceutical industry, or an equivalent combination of education and experience to successfully perform the key responsibilities of the job.
- Knowledge of CDISC requirements.
- Business fluency in English – both spoken and written – is a must.
Learn more about our EEO & Accommodations request here.
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Statistical Programmer II - Sponsor Dedicated employer: Fortrea
Contact Detail:
Fortrea Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Statistical Programmer II - Sponsor Dedicated
✨Tip Number 1
Network like a pro! Reach out to professionals in the industry on LinkedIn or at local meetups. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream job.
✨Tip Number 2
Prepare for interviews by practising common questions and scenarios related to statistical programming. We recommend doing mock interviews with friends or using online platforms to boost your confidence and refine your answers.
✨Tip Number 3
Showcase your skills! Create a portfolio of your SAS programming projects or any relevant work you've done. This gives potential employers a tangible look at what you can bring to the table, making you stand out from the crowd.
✨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, we love seeing candidates who are proactive about their job search!
We think you need these skills to ace Statistical Programmer II - Sponsor Dedicated
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the job description. Highlight your SAS programming experience and any relevant projects you've worked on in the clinical trials space.
Craft a Compelling Cover Letter: Use your cover letter to tell us why you're the perfect fit for the Statistical Programmer II role. Share specific examples of how you've led studies or tackled challenges in previous roles to show off your expertise.
Showcase Your Technical Skills: Don’t forget to mention your knowledge of CDISC requirements and any programming languages you’re proficient in. We want to see how you can contribute to our team right from the get-go!
Apply Through Our Website: For the best chance of success, make sure to apply through our website. It’s the easiest way for us to keep track of your application and get back to you quickly!
How to prepare for a job interview at Fortrea
✨Know Your SAS Inside Out
Make sure you brush up on your SAS programming skills before the interview. Be prepared to discuss your experience with developing SDTM and ADaM datasets, as well as any specific projects you've worked on that demonstrate your expertise.
✨Understand Clinical Trials
Familiarise yourself with the phases of clinical trials and the role of a Statistical Programmer within them. Being able to speak knowledgeably about how you can contribute to the success of complex studies will impress your interviewers.
✨Prepare for Technical Questions
Expect technical questions related to programming and data management. Practice explaining your thought process when tackling programming challenges, and be ready to showcase your problem-solving skills with real examples from your past work.
✨Showcase Your Communication Skills
Since you'll be interacting with various departments and clients, highlight your ability to communicate effectively. Prepare examples of how you've successfully collaborated with others in previous roles, especially in high-pressure situations.
