At a Glance
- Tasks: Lead statistical programming for clinical trials, ensuring compliance and quality in data management.
- Company: Join a forward-thinking company dedicated to advancing clinical research.
- Benefits: Attractive salary, flexible working options, and opportunities for professional growth.
- Other info: Collaborative team environment with a focus on continuous improvement and innovation.
- Why this job: Make a real difference in healthcare by managing critical clinical trial data.
- Qualifications: Experience in statistical programming and a strong understanding of clinical trial processes.
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.
Senior Statistical Programmer in Manchester employer: Tech Observer
As a Principal Biostatistician at our company, you will thrive in a collaborative and innovative work culture that prioritises employee growth and development. We offer competitive benefits, including flexible working arrangements and opportunities for professional advancement, all set in a vibrant location that fosters creativity and teamwork. Join us to make a meaningful impact in clinical research while enjoying a supportive environment that values your contributions.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Statistical Programmer in Manchester
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Some tips for your application 🫡
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How to prepare for a job interview at Tech Observer
✨Brush Up on Lab Techniques
Since you're eyeing a full-time gig in biotechnology, make sure you're well-versed in the lab techniques relevant to the role. Be ready to talk about PCR, CRISPR, or any specific methods mentioned in the job description at Tech Observer. You might even be asked to demonstrate your understanding of these processes.
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