At a Glance
- Tasks: Manage programming for clinical trials and ensure timely, accurate execution of projects.
- Company: Leading multinational Pharma client offering a fully remote role.
- Benefits: Competitive salary, flexible work environment, and opportunities for professional growth.
- Other info: Ideal for those passionate about clinical research and data analysis.
- Why this job: Join a dynamic team and contribute to impactful drug development projects.
- Qualifications: Bachelor's or Master's in Science/Statistics with relevant programming experience.
The predicted salary is between 50000 - 70000 € per year.
PE Global are currently recruiting for a Statistical Programming Manager for a 23 month contract role with a leading multinational Pharma client based in Harlow – Fully remote within the UK. The Clinical Programming is responsible for providing comprehensive programming support, including managing the timely and accurate execution of programming components of clinical trials. The clinical programming contractor independently manages completed projects that involve global tasks or cross functional teams. The role may require providing inputs to design and analysis, and reporting the results of clinical trials, including programming rules and mocked T/L/G. In addition, providing programming support for publication for our marketed drugs.
Job Responsibilities
- Primarily works at the Study, product/program level.
- Provides comprehensive programming support, including development of programs, ADaM specifications, analysis (datasets, TLFs) complying with regulatory requirements, departmental SOPs and work practices.
- Manages and delivers assignments with good quality and within timelines.
- Provides programming support to CDISC based e-submission.
- Develop, debug, and enhance SAS programs to support quality control of safety or efficacy derived datasets and TLFs.
- Implement programming standards and comply with regulatory requirements among project team members and across all projects; communicate to management on project status and resource gaps.
- Responsible for the standardization of GSD deliverables (TLGs, Datasets) across study projects within an indication/therapeutic area.
- Provides input on opportunities for process improvement.
- Proactively communicates issues impacting programming deliverables with Stat or DM team members.
Requirements
- Bachelor’s Degree/Master’s Degree in Science, Statistics, Information Technology or equivalent combination of education and related work experience.
- Bachelors + 5 years, Masters + 4 years of professional experience in a pharmaceutical or clinical research setting as a programmer.
- Proficient knowledge of clinical trials and drug development process, industry standards, statistical concepts used in analysis and submissions of clinical trial data.
- Strong understanding of SDTM, ADaM standards and Implementation guides.
- Demonstrated proficiency in using SAS to produce analysis datasets, TLFs, eSUB components and using other software applications (e.g. Pinnacle 21, XML and MS Office).
- Demonstrated ability to work independently and in a team environment.
Interested candidates should submit an updated CV.
Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in the UK.
Statistical Programmer in Warrington employer: PE Global
PE Global is an exceptional employer, offering a fully remote role as a Statistical Programming Manager with a leading multinational Pharma client based in Harlow. Our work culture prioritises collaboration and innovation, providing employees with ample opportunities for professional growth and development within the dynamic field of clinical trials. Join us to be part of a team that values quality, compliance, and continuous improvement, all while enjoying the flexibility of remote work in the UK.
StudySmarter Expert Advice🤫
We think this is how you could land Statistical Programmer in Warrington
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharma and clinical research sectors. A friendly chat can lead to opportunities that aren’t even advertised yet.
✨Tip Number 2
Show off your skills! Create a portfolio showcasing your programming projects, especially those related to SAS and clinical trials. This will give potential employers a taste of what you can do.
✨Tip Number 3
Prepare for interviews by brushing up on common statistical programming questions. We recommend practising with a friend or using mock interview platforms to build your confidence.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Statistical Programmer in Warrington
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Statistical Programmer role. Highlight relevant experience in clinical trials, programming skills, and any specific software you've used like SAS. We want to see how your background fits with what we're looking for!
Showcase Your Skills:Don’t just list your skills; demonstrate them! Use examples from your past work to show how you’ve applied your knowledge of SDTM, ADaM standards, and programming support. This helps us see your practical experience in action.
Be Clear and Concise:When writing your application, keep it clear and to the point. Avoid jargon unless it's relevant to the role. We appreciate straightforward communication that gets right to the heart of your qualifications and experiences.
Apply Through Our Website:We encourage you to apply through our website for a smoother process. It helps us keep track of applications and ensures you’re considered for the role. Plus, it’s super easy to do!
How to prepare for a job interview at PE Global
✨Know Your Programming Inside Out
Make sure you brush up on your SAS skills and be ready to discuss how you've used it in past projects. Be prepared to explain your understanding of ADaM and SDTM standards, as well as any relevant programming rules you've implemented.
✨Showcase Your Project Management Skills
Since the role involves managing projects independently, think of examples where you've successfully delivered assignments on time and with high quality. Highlight your experience with cross-functional teams and how you’ve communicated project statuses effectively.
✨Understand the Clinical Trial Landscape
Familiarise yourself with the drug development process and be ready to discuss how your programming work fits into clinical trials. This will show that you understand the bigger picture and can contribute meaningfully to the team.
✨Prepare for Process Improvement Discussions
Think about any opportunities for process improvements you've identified in your previous roles. Be ready to share these insights during the interview, as it demonstrates your proactive approach and commitment to enhancing programming deliverables.
