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 Portsmouth 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, while enjoying the flexibility of remote work in the UK.
StudySmarter Expert Advice🤫
We think this is how you could land Statistical Programmer in Portsmouth
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharma and clinical research sectors. Attend industry events or webinars, and don’t be shy about asking for introductions. We all know that sometimes it’s not just what you know, but who you know!
✨Tip Number 2
Prepare for those interviews! Research the company and its projects thoroughly. We recommend practising common interview questions related to statistical programming and clinical trials. Show them you’re not just a fit on paper, but also in person!
✨Tip Number 3
Showcase your skills! Create a portfolio of your programming projects or any relevant work you've done. This can really set you apart from other candidates. We love seeing practical examples of your expertise in SAS and clinical data analysis.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we often have exclusive roles listed there that you won’t find anywhere else. Don’t miss out on your dream job!
We think you need these skills to ace Statistical Programmer in Portsmouth
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Statistical Programmer role. Highlight your experience with SAS, clinical trials, and any relevant programming standards like SDTM and ADaM. We want to see how your skills match what we're looking for!
Showcase Your Experience:When writing your application, don’t just list your previous jobs. Instead, showcase specific projects or tasks where you’ve managed programming components of clinical trials. We love seeing real examples of your work!
Be Clear and Concise:Keep your application clear and to the point. Use bullet points for easy reading and make sure to communicate your key achievements in a straightforward manner. We appreciate clarity as much as you do!
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. We can’t wait to see what you bring to the table!
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 your experience with ADaM specifications and TLFs. Be prepared to explain how you've applied these in past projects, as this will show your practical knowledge and ability to deliver quality results.
✨Understand the Clinical Trial Landscape
Familiarise yourself with the clinical trials and drug development process. Knowing the ins and outs of SDTM and ADaM standards will help you answer questions confidently and demonstrate your expertise in the field.
✨Showcase Your Problem-Solving Skills
Be ready to discuss specific challenges you've faced in previous roles and how you overcame them. This could involve programming issues or project management hurdles. Highlighting your proactive communication with teams can also set you apart.
✨Prepare Questions for Them
Think of insightful questions to ask about their programming standards and team dynamics. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.
