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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 presence in over 20 countries.
- Benefits: Enjoy flexible working options, competitive salary, and opportunities for professional growth.
- Why this job: Be part of a dynamic team that values innovation and continuous improvement in healthcare.
- Qualifications: Experience in statistical programming and knowledge of GCP and CDISC standards required.
- Other info: We are hiring 20+ positions, offering a chance to make a real impact in clinical research.
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 the field.
✨Tip Number 3
Showcase your problem-solving skills by preparing examples of how you've tackled challenges in previous roles. Be ready to discuss specific scenarios where you improved processes or resolved issues, as this is a key aspect of the role.
✨Tip Number 4
Research Tech Observer's projects and values to tailor your discussions during interviews. Understanding their approach to clinical trials and data management will allow you to align your experiences with their needs, making you a more attractive candidate.
We think you need these skills to ace Principal/Senior Statistical Programmer
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the Principal/Senior Statistical Programmer position. Familiarise yourself with key terms like CDISC, GCP, and SAS programming to demonstrate your knowledge in your application.
Tailor Your CV: Customise your CV to highlight relevant experience in statistical programming, clinical trials, and adherence to industry standards. Use specific examples that showcase your skills in SAS programming and your understanding of GCP and FDA guidelines.
Craft a Strong Cover Letter: Write a compelling cover letter that outlines your passion for clinical research and your expertise in statistical programming. Mention how your background aligns with Tech Observer's mission and values, and express your enthusiasm for contributing to their projects.
Proofread Your Application: Before submitting, carefully proofread your application materials for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in the field of statistical programming.
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 knowledge and ability to adhere to industry standards.
✨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 skills, as these are crucial for a Principal/Senior Statistical Programmer role.
✨Understand the Role of Team Collaboration
Be ready to discuss your experience working in teams, especially in cross-functional settings. Emphasise your ability to represent statistical programming in meetings and how you contribute to team success.
✨Demonstrate Continuous Improvement Mindset
Talk about how you have contributed to the improvement of processes in your previous positions. Mention any feedback you've provided on SOPs and how you stay updated with new programming techniques and IT developments.
