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- Tasks: Develop clinical study reports using SAS programming for regulatory submissions.
- Company: IQVIA is a global leader in clinical research and healthcare intelligence.
- Benefits: Enjoy remote work, cutting-edge technology, and opportunities for career development.
- Why this job: Join a fast-paced, collaborative team making a real impact on global health.
- Qualifications: Master’s or Bachelor’s in Biostatistics, Statistics, Mathematics, or Computer Science required.
- Other info: Embrace your curiosity and grow your career with us!
The predicted salary is between 36000 - 60000 £ per year.
IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory submissions. Programming and performing related tasks serving the full spectrum of statistical programming needs in our DS3 environment (home based):
- Import data from various sources
- Program quality control checks for source data and reporting data issues
- Interpret project level requirements and develop programming specifications
- Write programming code following established Good Programming Practices
- Program ADaM datasets
- Program to create statistical analysis tables, listings and figures
- Validate datasets and all statistical outputs per prescribed gate checks
- Communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and timelines
- Use and promote the use of established standards, SOPs, and standard methodologies
- Export data and clinical study report materials
- Provide training and mentoring to team members and department staff
You can help us bring clinical trial statistical analysis into the next generation. Award winning and innovative, we will give you access to cutting-edge in-house technology, allowing you to work on global projects across therapeutic areas. Be challenged in a fast-paced team environment that is collaborative in performing biostatistical analyses and advanced statistical programming. Development opportunities and mentoring at all levels enable you to progress your long-term career in the direction you choose.
THE PERSON
We know that meaningful results require not only the right approach, but also the right people. Candidates should possess a Master’s or Bachelor’s degree in Biostatistics, Statistics, Mathematics, or Computer Science, and have a strong educational or practical evidence in programming. Key required skills include:
- Home Based/Remote
- 5+ years experience in Statistical Programmer role from CRO/Pharma with ADaM and TFL
- Excellent accuracy, attention to detail, problem solving, organizational as well as interpersonal communication.
- Experience in programming in SAS within the CRO/Pharma/Biotech/Healthcare industries
- Knowledge of statistics and exhibit routine and occasionally complex analytical skills
- A focus on quality, accuracy, and completeness of work activities
- Excellent communication skills
- A good understanding of Good Clinical Practice and ICH guidelines
- Ability to independently lead (or have lead potential) and estimate programming scope of work, handle resource assignments, communicate work status, and work within project timelines for deliverables
- Take initiative and can be counted on to get the job done, with integrity
- Have the self-awareness to recognize when negotiating skills and assistance are needed
- Ability to establish and maintain effective working relationships with co-workers, managers, and clients
Embrace your curiosity and grow your career in an exciting environment where development is a priority. Think boldly and disrupt conventional thinking. Enjoy what you do. Discover a career with greater purpose and help create a healthier world. Whatever your career goals, we are here to ensure you get there!
Senior Statistical Programmer employer: CTI Clinical Trial and Consulting Services
Contact Detail:
CTI Clinical Trial and Consulting Services Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Statistical Programmer
✨Tip Number 1
Familiarise yourself with the latest SAS programming techniques and tools. Since the role requires strong SAS skills, consider taking online courses or certifications that focus on advanced statistical programming to enhance your expertise.
✨Tip Number 2
Network with professionals in the CRO and Pharma industries. Attend relevant webinars or conferences where you can meet current employees or recruiters from IQVIA. This can give you insights into the company culture and expectations.
✨Tip Number 3
Brush up on your knowledge of Good Clinical Practice (GCP) and ICH guidelines. Understanding these regulations is crucial for the role, so being able to discuss them confidently during interviews will set you apart.
✨Tip Number 4
Prepare to demonstrate your problem-solving skills through real-world examples. Think of specific instances where you've successfully tackled programming challenges or improved processes, as this will showcase your ability to handle the responsibilities of the role.
We think you need these skills to ace Senior Statistical Programmer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in statistical programming, particularly with SAS. Emphasise your familiarity with ADaM datasets and TFL, as these are key requirements for the role.
Craft a Strong Cover Letter: In your cover letter, express your passion for biostatistics and clinical trials. Mention specific projects or experiences that demonstrate your problem-solving skills and attention to detail, which are crucial for this position.
Showcase Your Technical Skills: Clearly outline your technical skills related to SAS programming and any other relevant software. Include examples of how you've used these skills in previous roles to solve complex problems or improve processes.
Highlight Communication Abilities: Since the role involves collaboration with statisticians and clinical teams, emphasise your interpersonal communication skills. Provide examples of how you've effectively communicated project requirements and timelines in past experiences.
How to prepare for a job interview at CTI Clinical Trial and Consulting Services
✨Showcase Your SAS Skills
Make sure to highlight your experience with the SAS programming language during the interview. Be prepared to discuss specific projects where you used SAS to develop clinical study report materials, and how you implemented quality control checks.
✨Demonstrate Attention to Detail
Given the importance of accuracy in statistical programming, be ready to provide examples of how you've ensured precision in your work. Discuss any methods or practices you follow to maintain high standards in your programming outputs.
✨Communicate Effectively
Since the role involves collaboration with statisticians and clinical team members, practice articulating your thoughts clearly. Prepare to discuss how you’ve successfully communicated project requirements and timelines in past roles.
✨Emphasise Problem-Solving Skills
Be ready to share instances where you've encountered challenges in programming and how you resolved them. Highlight your analytical skills and your ability to think critically under pressure, as these are key for the role.
