Real World Evidence (RWE) Programmer
This is the employer's own posting, not a copy on a job board.
What we know
Is it still open?
Confirmed still open
Last checked 1d ago — checked against the employer's own applicant tracking system, which is the company answering directly.
We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.
How old is it?
Posted 48d ago
The date the source published, not the day we noticed it (2026-07-29). Last seen at its source 2h ago.
Is it remote?
Marked remote on the employer's board
Their board carries a remote setting on this posting — a field they filled in, not wording we read. The location field names somewhere specific, which is usually where the team or the entity sits.
Who may apply?
United Kingdom, South Africa, Poland
The description states no restriction of its own. This is the source's own tag.
Pay not stated
Similar roles pay £75k–120k/yr
Middle 50% of 61 listings that do state pay — Engineering · all levels · United Kingdom · GBP/year. This employer has published no salary; this is what comparable listings we hold disclose, never converted between currencies or periods. How this is calculated.
Skills named in the ad
Recognised terms only, from a fixed vocabulary — this is what CV matching compares against.
Carried by 1 source
-
workable employer's own board first seen 11d ago · last seen 2h ago
The listing
Unlock Your Future in Life Sciences Programming at Quanticate!
Are you a skilled SAS Programmer with a strong grasp of SQL? Ready to leverage your technical expertise in impactful Real World Evidence (RWE) life science projects rather than finance or other industries? Join Quanticate, one of the world's leading data-focused CROs, where you’ll contribute to some of the most advanced clinical programs across the globe.
Be a part of projects that contribute to the advancement of therapies that genuinely make a difference in patients' lives.
Our customers range from top global pharmaceutical companies where you can work as an integrated team member on a world leading clinical program, to small biotech’s that are taking their first steps in clinical development
We strongly advocate career development providing membership to professional societies, encouraging your involvement in their activities and committees. Together we can help you build the career you want – developing your skills, working on challenging problems, to ultimately develop clinical therapies that matter.
Procedures:
- Program tables, figures and listings and derived datasets according to the request description.
- Perform quality control checks and complete quality control documentation for programming plans, specifications, outputs/derived datasets.
- Perform other reasonable programming tasks as requested by management.
- Follow appropriate Project Management procedures.
- Communicate effectively with OR team.
- Provide input to improvements to processes, procedures and standards.
- Support the training and development of other programmers.
Objectives:
- Further development of knowledge of SAS and advanced SQL, good programming practices and numerous Real World Data (RWD) databases.
- Ensure high levels of customer care are provided.
- Review available resources to find required information
- Use and manipulate data stored in SQL database.
- Ability to understand and modify SAS macros.
- Use longitudinal databases (Administrative medical and pharmacy claims databases, Electronic Medical Records).
- Technical experience in handling large datasets.
- Basic understanding of statistical models used in Outcomes Research (OR)
- Ability to ask questions effectively.
Requirements
- Good knowledge of statistical software packages (particularly SAS),
- Good knowledge of SQL
- Qualified to degree level or equivalent, preferably in a numerate discipline.
- Should have PC skills
- Good organisational skills, communication skills (oral and written)
- Good analytical skills and attention to detail.