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- Tasks: Join us as a Principal/Senior Statistical Programmer, ensuring quality in clinical trial data management.
- Company: Tech Observer is a global leader in clinical research with a diverse international presence.
- Benefits: Enjoy flexible working options, competitive salary, and opportunities for professional growth.
- Why this job: Be part of a dynamic team making a real impact in healthcare through innovative data solutions.
- Qualifications: Experience in statistical programming and knowledge of GCP and CDISC standards are essential.
- Other info: We're hiring 20+ positions, offering a chance to work on exciting global projects.
The predicted salary is between 48000 - 84000 £ per year.
Tech Observer is a global Clinical Research Organization (CRO) and Functional Service Provider (FSP) headquartered in New Jersey, USA, with a strong presence in India, Singapore, the UK, Denmark, and over 20 other countries. We are currently hiring for the positions of Senior Statistical Programmers and Principal programmers on FSP in the United Kingdom. No. of Positions 20+.
Key Responsibilities:
- Compliance with working SOPs within the framework of the Quality Management System and to Good Clinical Practice (GCP).
- Ensure adherence to programming guidelines.
- Implement and follow the latest versions of CDISC, FDA Guidelines, GCP and other industry standards.
- Participate in and co-ordinate the Statistical Programming review of Case Report Forms (CRFs), annotated CRFs, database structures and study related documentation (e.g. data validation guidelines).
- Review and interpret Report and Analysis Plans and provide comments for assigned projects.
- Develop and review SAS programs and output for the management of clinical trial data, the tabulation of data, preparation of patient data listings, graphical output, and creation of derived datasets and statistical analysis of data as specified in the Statistical or Report Analysis Plans.
- Develop SAS programs for ad hoc tables and listings.
- Write, modify, and maintain programs that produce diagnostics and listing for data review in support of Data Management.
- Carry out electronic data transfer (both incoming and outgoing).
- Develop and review programs to ensure the data transfer has been produced to specification.
- Design and set-up utilities/SAS based systems to assist and facilitate Clinical Data Management activities.
- Review draft and final production runs for projects to ensure quality and consistency.
- Provide feedback for continuous improvement of SOPs from BPP and other cross functional SOPs.
- Ensure quality of personal work and the work of the team when acting as a Lead Programmer or Biometrics Project Manager.
- Assume team member responsibilities, including representing Statistical Programming at internal project team meetings, client meetings and audits.
- With sufficient experience may support the activities of senior Statistical Programming staff by providing input into time and cost estimates and presentations to clients.
- Advise Senior Statistical Programming staff of changes in scope of projects to enable the timely development of change orders.
- Demonstrate excellent problem solving skills, a proactive approach and a willingness to take decisions on a regular basis.
- Encourage and participate in the ongoing review of the processes used by the Statistical Programming group to ensure processes are continually improved.
- Maintain awareness of new developments in programming techniques and IT which may be applied to the management and reporting of clinical trial data.
- Perform other duties as assigned by senior Statistical Programming staff.
Principal/Senior Statistical Programmer employer: Tech Observer
Contact Detail:
Tech Observer Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Principal/Senior Statistical Programmer
✨Tip Number 1
Familiarise yourself with the latest CDISC and FDA guidelines, as well as Good Clinical Practice (GCP) standards. This knowledge will not only help you in interviews but also demonstrate your commitment to compliance and quality in statistical programming.
✨Tip Number 2
Network with professionals in the clinical research field, especially those who work as statistical programmers. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends and technologies in statistical programming.
✨Tip Number 3
Showcase your problem-solving skills by preparing examples of how you've tackled challenges in previous projects. Be ready to discuss these scenarios during interviews to highlight your proactive approach and decision-making abilities.
✨Tip Number 4
Stay updated on new programming techniques and IT developments relevant to clinical data management. Mention any recent tools or software you've learned about in your conversations with recruiters, as this shows your dedication to continuous improvement.
We think you need these skills to ace Principal/Senior Statistical Programmer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in statistical programming, particularly with SAS and clinical trial data management. Emphasise your familiarity with CDISC, GCP, and FDA guidelines, as these are crucial for the role.
Craft a Strong Cover Letter: In your cover letter, express your enthusiasm for the position and the company. Mention specific projects or experiences that demonstrate your problem-solving skills and proactive approach, which are key attributes for this role.
Showcase Technical Skills: Clearly outline your technical skills related to statistical programming and data analysis. Include any relevant certifications or training that support your expertise in SAS programming and clinical data management.
Highlight Team Collaboration: Since the role involves working closely with other team members and clients, provide examples of past experiences where you successfully collaborated on projects. This will show your ability to work effectively in a team environment.
How to prepare for a job interview at Tech Observer
✨Know Your Programming Standards
Familiarise yourself with CDISC, FDA Guidelines, and GCP standards. Be prepared to discuss how you have implemented these in your previous roles, as this will demonstrate your compliance and understanding of industry expectations.
✨Showcase Your Problem-Solving Skills
Prepare examples of how you've tackled complex programming challenges in the past. Highlight your proactive approach and decision-making abilities, as these are crucial for a Principal/Senior Statistical Programmer role.
✨Understand the Role of Team Dynamics
Be ready to discuss your experience in leading teams or projects. Emphasise your ability to collaborate effectively with cross-functional teams and how you contribute to continuous improvement within the group.
✨Prepare for Technical Questions
Expect technical questions related to SAS programming and data management. Brush up on your technical skills and be ready to explain your thought process when developing and reviewing SAS programs.
