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- Tasks: Develop and execute SAS programs for clinical data analysis and validation.
- Company: Join a pioneering global CRO dedicated to improving lives through innovative research.
- Benefits: Remote work, competitive salary, and opportunities for professional growth.
- Other info: Inclusive environment that values diverse talent and fosters collaboration.
- Why this job: Make a real impact in healthcare by working on cutting-edge clinical trials.
- Qualifications: Degree level education with advanced SAS programming skills required.
The predicted salary is between 30000 - 50000 £ per year.
Statistical Programmer 1 – Europe – Remote
Join to apply for the Statistical Programmer 1 – Europe – Remote role at Worldwide Clinical Trials
Overview
We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, a global team of over 3,500+ experts who are changing the way the world experiences CROs – in the best possible way. Our mission is to work with passion and purpose every day to improve lives, and we are looking for others who share this pursuit.
What Global Programming Does At Worldwide
The Worldwide team is an experienced and diverse group of Programmers who collaborate together as one, both via regularly scheduled group meetings to discuss issues, and impromptu one-on-one discussions between colleagues to discuss a particular topic. As a Statistical Programmer on a project – you will be working with statisticians, sponsors, the wider study team and your own team of programmers, ensuring the data and output delivered for a study meets industry, regulatory submission and quality standards. As a Statistical Programmer at Worldwide, your analytical skills and ability to both program and understand / interpret data are the keys to success, and you will have the opportunity to continually grow your knowledge in SAS and CDISC across all phases and multiple therapy areas.
What You Will Do
- Develop, test and execute SAS programs to produce and validate CDISC SDTM and ADaM datasets, tables, figures and listings (TFL).
- Perform review and provide guidance on the development of the clinical database specification, data transfer agreement/specification, specification of tables, figures and listings (TFL) shells.
- Develop and review specification for SDTM datasets and ADaM datasets for safety data, TFL shells and other specifications, e.g. patient profiles, OPS reports.
- Develop and review electronic data submission package (SDTM annotated CRF, define.xml, Study/Analysis Data Reviewer\’s Guide) for high complexity studies.
What You Will Bring To The Role
- Must be computer literate and numerate with a willingness to adapt to various computer systems.
- Hands-on expert level project statistical programmer experienced in providing programming leadership to projects.
- Statistical programming skills and knowledge across a broad range of applications together with key competencies in customer focus, delivering on commitments, building strong relationships, communicating and influencing, and embracing innovation and change.
Your Experience
- Educated to degree level or equivalent.
- Advanced SAS programming skills with expert knowledge in SAS/Macro, Proc Report and ODS. Good working knowledge in SAS/Graph, Proc SQL, SAS/STAT.
Equal Opportunity
Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.
Details
- Seniority level: Mid-Senior level
- Employment type: Full-time
- Job function: Research, Analyst, and Information Technology
- Industries: Research Services
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Statistical Programmer 1 - Europe - Remote employer: Worldwide Clinical Trials
Contact Detail:
Worldwide Clinical Trials Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Statistical Programmer 1 - Europe - Remote
✨Tip Number 1
Network like a pro! Reach out to current or former employees at Worldwide Clinical Trials on LinkedIn. A friendly chat can give you insider info and might just lead to a referral.
✨Tip Number 2
Prepare for the interview by brushing up on your SAS skills and understanding CDISC standards. We want to see your analytical prowess in action, so be ready to discuss your past projects and how you tackled challenges.
✨Tip Number 3
Show your passion for improving lives! During interviews, share why you’re excited about the role and how your skills can contribute to the mission of Worldwide Clinical Trials. Authenticity goes a long way!
✨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, it shows you’re serious about joining our innovative team.
We think you need these skills to ace Statistical Programmer 1 - Europe - Remote
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Statistical Programmer role. Highlight your SAS programming skills and any relevant experience in clinical trials. We want to see how your background aligns with what we do at Worldwide Clinical Trials!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about statistical programming and how you can contribute to our mission. Let us know what excites you about working with a global team like ours.
Showcase Your Analytical Skills: In your application, don’t forget to showcase your analytical skills and any projects where you've successfully interpreted data. We love seeing examples of how you've tackled challenges in the past!
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It’s the best way for us to receive your application and get you on our radar. Plus, it shows you’re keen on joining our innovative team!
How to prepare for a job interview at Worldwide Clinical Trials
✨Know Your SAS Inside Out
Make sure you brush up on your SAS programming skills before the interview. Be ready to discuss specific projects where you've used SAS, especially in developing SDTM and ADaM datasets. This will show that you not only understand the theory but can also apply it practically.
✨Understand the Role of a Statistical Programmer
Familiarise yourself with the responsibilities of a Statistical Programmer at Worldwide Clinical Trials. Be prepared to talk about how you would collaborate with statisticians and other team members, and how your analytical skills can contribute to the success of clinical trials.
✨Prepare for Technical Questions
Expect technical questions related to SAS, CDISC standards, and data validation processes. Practise explaining complex concepts in simple terms, as this will demonstrate your ability to communicate effectively with both technical and non-technical stakeholders.
✨Show Your Passion for Innovation
Worldwide Clinical Trials values creativity and innovation. Think of examples from your past work where you took a unique approach to problem-solving or improved a process. Sharing these stories will highlight your alignment with their mission and culture.