Statistical Programmer at Siloah St Trudpert Klinikum
berlin, Berlin, Germany -
Full Time


Start Date

Immediate

Expiry Date

19 Jan, 27

Salary

85000.0

Posted On

21 Oct, 26

Experience

1 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Industry

Medical Practices & Clinics

Description

About the job

Senior Statistical Programmer | CRO | Germany | Remote | Permanent

We are working with an established international specialist biometrics CRO seeking an experienced Senior Statistical Programmer to join its expanding team in Germany.

With over 30 years of experience and more than 150 employees, the organisation supports pharmaceutical and biotechnology clients globally, delivering specialist services across biostatistics, statistical programming, clinical data management and medical writing.

This opportunity offers the chance to work on a diverse range of clinical studies within a collaborative, technically driven environment that values quality, professional development and long-term career progression.

  • Key ResponsibilitiesDevelop, program and validate clinical trial datasets and statistical analyses using SAS.
  • Create and maintain CDISC SDTM and ADaM datasets.
  • Produce and quality-check Tables, Listings and Figures (TLFs).
  • Ensure programming deliverables meet quality standards and project requirements.
  • Support statistical programming activities across the clinical study lifecycle.
  • Work closely with statisticians, data management teams and other clinical research professionals.


  • Requirements5+ years' statistical programming experience within clinical research, preferably in a CRO or pharmaceutical organisation.
  • Advanced SAS programming skills.
  • Strong practical experience with CDISC SDTM and ADaM standards – essential.
  • Experience programming and validating clinical trial datasets and statistical outputs.
  • R programming experience would be beneficial.
  • Degree in Statistics, Mathematics, Computer Science, Medical Biometrics or a related discipline.
  • Excellent English communication skills and a collaborative approach.


  • What's on OfferFlexible working arrangements, including remote, hybrid or office-based options.
  • Competitive salary and benefits.
  • Supportive, international working environment with flat hierarchies.
  • Exposure to varied clinical research projects.
  • Structured onboarding, ongoing training and professional development.
  • Long-term career opportunities within an established and growing CRO.


Interested?For further information or a confidential discussion, please contact Jo Fornaciari at jo@warmanobrien.com.

Applicants must already have the right to work in Germany. Visa sponsorship is not available.

We also support other opportunities across pharmaceutical, biotechnology and CRO organisations throughout Europe. Please reach out to arrange a confidential discussion.


Responsibilities

About the job

Senior Statistical Programmer | CRO | Germany | Remote | Permanent

We are working with an established international specialist biometrics CRO seeking an experienced Senior Statistical Programmer to join its expanding team in Germany.

With over 30 years of experience and more than 150 employees, the organisation supports pharmaceutical and biotechnology clients globally, delivering specialist services across biostatistics, statistical programming, clinical data management and medical writing.

This opportunity offers the chance to work on a diverse range of clinical studies within a collaborative, technically driven environment that values quality, professional development and long-term career progression.

  • Key ResponsibilitiesDevelop, program and validate clinical trial datasets and statistical analyses using SAS.
  • Create and maintain CDISC SDTM and ADaM datasets.
  • Produce and quality-check Tables, Listings and Figures (TLFs).
  • Ensure programming deliverables meet quality standards and project requirements.
  • Support statistical programming activities across the clinical study lifecycle.
  • Work closely with statisticians, data management teams and other clinical research professionals.


  • Requirements5+ years' statistical programming experience within clinical research, preferably in a CRO or pharmaceutical organisation.
  • Advanced SAS programming skills.
  • Strong practical experience with CDISC SDTM and ADaM standards – essential.
  • Experience programming and validating clinical trial datasets and statistical outputs.
  • R programming experience would be beneficial.
  • Degree in Statistics, Mathematics, Computer Science, Medical Biometrics or a related discipline.
  • Excellent English communication skills and a collaborative approach.


  • What's on OfferFlexible working arrangements, including remote, hybrid or office-based options.
  • Competitive salary and benefits.
  • Supportive, international working environment with flat hierarchies.
  • Exposure to varied clinical research projects.
  • Structured onboarding, ongoing training and professional development.
  • Long-term career opportunities within an established and growing CRO.


Interested?For further information or a confidential discussion, please contact Jo Fornaciari at jo@warmanobrien.com.

Applicants must already have the right to work in Germany. Visa sponsorship is not available.

We also support other opportunities across pharmaceutical, biotechnology and CRO organisations throughout Europe. Please reach out to arrange a confidential discussion.


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