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Senior Programmer I/II (Real World Data/Evidence)

Posted 26 days ago

RemoteUnited KingdomSE

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.

This is a fully remote role but candidates must be based in UK or Poland due to employment contracts.

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

  • Extensive knowledge of statistical software packages (particularly SAS),
  • Extensive knowledge of SQL
  • Qualified to degree level or equivalent, preferably in a numerate discipline.
  • Experience with large datasets, ideally, Medical data - Healthcare databases, Payer databases, Hospital records
  • Should have PC skills
  • Good organisational skills, communication skills (oral and written)
  • Good analytical skills and attention to detail.

Benefits

  • Private medical care
  • Life insurance
  • Flexible working time
  • Full time home working
Job details
Workplace
Remote
Location
United Kingdom
Experience
SE

A leading global Biometrics Clinical Research Organisation (CRO) dedicated to providing expertise in statistical analysis, data capture and clinical trial reporting

Employees
202
Industry
Research Services
Headquarters
Hitchin, Hertfordshire
Founded
1994
Company location
Bevan House, Bancroft Court, Hitchin, Hertfordshire SG5 1LH, GB
Specialties
Clinical Research, Biometrics, Statistics, Programming, Medical Communications, Clinical Data Management, Electronic Data Capture, Pharmacovigilance, SAS Programming, SDTM, and Automation

Key team members

Fabien Du Fraisse

Fabien Du Fraisse

Justyna Misiura

Justyna Misiura

Nicholas D.

Nicholas D.

Shrikrishna Shroff

Shrikrishna Shroff

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