Statistical Programmer II - RWE

I am working with a market leading global CRO who are committed to bringing life changing drugs and therapies to quickly to market and have an exciting opportunity for a Statistical Programmer II to join them in their RWE Team. If you are interested in working alongside a group of diverse, talented people that work daily on making a real positive impact on human lives and overcoming some of the biggest challenges facing global public health this may be the role for you!

This is an exciting new solution-driven role as Real World Evidence expands into developing further innovations for clients.  This is a fully home-based role that can be based in the UK or across Europe.

What you will be doing:

• Provide statistical programming and data harmonization (for primary and secondary data from multiple sources - EMRs, PROs, eCRF, Observational studies, etc.) support & expertise.
• Advise on database design, data collection and programme tables, listings and figures using SAS (Base SAS, SAS/STAT and SAS Macro) and other applications.
• Conduct statistical analyses for client reports and publications.
• Develop, implement, and validate new process technologies, macros and applications under supervision.
• Utilise innovative insights for solution, operations, and product development.
• Work directly with both external and internal clients.
• Perform programming quality control checks for source data and report issues.
• Review, detect and correct TLFs, edit checks and SAS programs to ensure quality.
• Assist in the development of programming documentation including specifications.
• Provide technical expertise and project solutions.
• Fulfil project responsibilities at the level of assisting the statistical programming Team Lead.
• Work independently, act as technical lead and plan from time to time when required.

What you will need to have:

• MSC/BSC in computer science or relevant in health-related field.
• Knowledge of statistics, programming, and clinical drug development process.
• Working knowledge of Base SAS, SAS/STAT and SAS Macro Language.
• 2 years working knowledge of the ADaM standards and TLFs in clinical trials.
• Working knowledge of the SDTM structure.
• Ability to estimate programming scope of work and implement programming specifications.
• Excellent accuracy, attention to detail, organizational, interpersonal and communication skills.
• Ability to establish working relationships with co-workers, managers, and clients.
• In-depth knowledge of applicable clinical research regulatory requirements would be an advantage, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guideline

What’s in it for you:

• Opportunity to work with the leading international healthcare organizations and the latest healthcare trends.
• Progress and shape your long-term career in the direction you choose.
• Access to industry-leading data and experts, you will find endless opportunities for growth.
• Excellent salary and extensive benefits package.
• Annual performance related bonus.
• Flexible working hours & healthy work life balance.
• Excellent training and development to give a clear career development path.

What to do next:

If this opportunity is of interest, please apply now with your CV as the organisation are looking to welcome the new Statistical Programmer onboard as soon as possible.

Not what you’re looking for?  

Please contact Jo Fornaciari on 07810 090 785 for a confidential discussion about potential opportunities.