At a Glance
- Tasks: Manage clinical trial data and ensure compliance with SDTM standards.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Remote work options, competitive salary, and opportunities for professional growth.
- Other info: Dynamic role with excellent career advancement opportunities across Europe and South Africa.
- Why this job: Make a real impact on patient outcomes while working with innovative technologies.
- Qualifications: Experience in SAS programming and knowledge of clinical data management required.
The predicted salary is between 54000 - 66000 £ per year.
This unique role within IQVIA lends itself to a technically minded person with strong communication skills and SDTM knowledge. Having experience in Study Design, CRF annotation, CDISC standards, Vendor management with SAS programming skills will be key for this position. The role can be based remotely from anywhere in Europe or in South Africa.
This role is part of a sponsor dedicated project where you will be working with the client directly to manage Database CRF and SDTM Deliveries. Responsibilities include:
- Management of CRF design from the protocol, ensuring Vendors specifications are compliant with SDTM needs.
- Defining SDTM specification on some studies and/or SDTM review and oversight, ensuring quality and completeness of SDTM format data.
- Collaboration with Study Data Leads to ensure planning for data receipt and its oversight throughout the duration of assigned clinical trials.
- Programming reports and contributing to the standardization of process and reports used for data review and analysis for external partners/vendors and internal teams.
- Completing formal and ad-hoc analyses and oversight of SDTM data.
- Reviewing critical documents/deliverables (SDTM Annotation, SDTM datasets) to ensure Data Standards are used consistently and support creation of DE dataset.
- Mapping SDTM data and managing annotated CRF.
- Attending meetings as applicable with various teams including Mission, Submission, Project, Program, JCST, DEM, Biometrics, Clinical & Regulatory Solutions Team (CRST), Early Phase.
- Performing relevant quality checks and creating standard edit checks for new CRF modules.
- Supporting audits and inspections as required and other responsibilities and projects that the Company may assign.
- Writing and reviewing technical specifications.
Experience required includes:
- Data mapping and SDTM Controlled Terminology.
- SAS programming and SDTM deliveries.
- Prior experience in a clinical or pharmaceutical related field.
- Prior experience in a Data Management related field.
- Experience with relational databases, preferably Clinical Data Management and EDC Systems.
- Advanced knowledge of federal regulations, Good Clinical Practice, and Good Clinical Data Management Practices.
- Excellent command, both verbal and written, of English.
Programmer (SAS - Clinical Trials) in Reading employer: IQVIA
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that prioritises innovation and employee well-being. Our South West England location provides flexible working arrangements, comprehensive well-being support, and robust career development opportunities through our AI-powered talent marketplace, ensuring that you can thrive both personally and professionally while contributing to meaningful advancements in healthcare.
StudySmarter Expert Advice🤫
We think this is how you could land Programmer (SAS - Clinical Trials) in Reading
✨Join Local Tech Meetups
Get out there and mingle with fellow developers by joining local tech meetups. It’s a fantastic way to meet people who might be working at IQVIA or know someone who does. Plus, you can pick up some trendy tech skills and trends while you're at it!
✨Contribute to Open Source Projects
Show off your coding chops by jumping into open-source projects. Not only does this give you practical experience, but it also gets you noticed in the dev community. You'll create a killer portfolio that speaks volumes about your skills to IQVIA.
✨Tap into Online Developer Communities
Don’t underestimate the power of online developer communities like GitHub, Stack Overflow, and even Reddit. Participate in discussions, share your projects, and build your visibility. We can often find opportunities through these channels that can lead to a full-time gig at companies like IQVIA.
✨Explore Job Boards Specifically for Tech Roles
Keep your eyes peeled on job boards that focus on tech roles. Sites like TechCareers or Stack Overflow Jobs can often have listings for companies like IQVIA that might not show up on broader job sites. Make it a habit to check these regularly, and don’t hesitate to apply directly through our website!
We think you need these skills to ace Programmer (SAS - Clinical Trials) in Reading
Some tips for your application 🫡
Show off your coding skills:When applying for a software engineering role, it's super important to showcase your coding skills. Make sure your CV includes your tech stack, any relevant programming languages you’re comfortable with, and examples of projects you've worked on. If you have a GitHub profile, link it up! We love to see code in action.
Tailor your portfolio:For a full-time role, we’d expect to see some solid examples of your work in your portfolio. Make sure to include at least two or three projects that highlight your problem-solving skills and your ability to work with different technologies. Focus on the projects that are most relevant to the position at IQVIA.
Craft a killer cover letter:Your cover letter is your chance to stand out—make it personal! Explain why you want to work at IQVIA and how your skills align with the role. Show us your passion for software development. We dig enthusiastic candidates who understand the value of collaboration and continuous learning!
Be clear and concise:When it comes to writing your CV and cover letter, clarity is key. Avoid jargon that could confuse us and stick to simple, direct language. Highlight your achievements with quantifiable results where possible, and keep everything easy to read. A well-organised application goes a long way!
How to prepare for a job interview at IQVIA
✨Brush Up on Your Coding Skills
For a full-time software engineering role, it's crucial that we stay sharp with our coding abilities. Expect technical questions that might involve solving problems on the spot or discussing algorithms. Practise on platforms like LeetCode or HackerRank to get comfortable with the types of questions that often come up.
✨Know Your Tools and Frameworks
Make sure we’re well-acquainted with the tools and technologies listed in the job description. Familiarise ourselves with any specific frameworks or programming languages mentioned. If IQVIA uses React or Node.js, for instance, be ready to discuss how we’ve used them in previous projects or coursework.
✨Showcase Your Projects
Bring along a portfolio that highlights our best work. This could be code samples, GitHub repositories, or any side projects we’ve built. Make sure we can talk through our thought process for each project, especially the challenges we faced and how we solved them—this shows our problem-solving skills in action.
✨Prepare for Behavioural Questions
While technical skills are key, full-time positions also require cultural fit. Be ready to discuss our previous experiences and how we handle teamwork, conflict, and deadlines. Brush up on the STAR method—Situation, Task, Action, Result—to clearly articulate our past experiences when discussing how we've contributed to a team.
