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Freelance Senior Principal Statistical programmer (m/f/x)

Progressive / SThree Group

Deutschland

Remote

EUR 60.000 - 80.000

Vollzeit

Gestern
Sei unter den ersten Bewerbenden

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Zusammenfassung

A leading recruitment firm is seeking a freelance Senior Principal Statistical Programmer to support a project in Global Medical Affairs for a renowned client in the life sciences sector. The role involves conducting statistical analyses, collaborating with stakeholders, and ensuring high-quality delivery. Ideal candidates will have a Bachelor's degree in a relevant field, strong programming skills in SAS and R, and at least some experience in clinical research. The position offers flexibility as it is 100% remote with a workload of 40 hours per week.

Qualifikationen

  • Bachelor's degree in related fields, Master's preferred.
  • Experience in clinical research or drug development.
  • Strong programming skills in SAS and R.

Aufgaben

  • Conduct statistical analyses for Global Medical Affairs.
  • Deliver outputs for publications, abstracts, presentations, and submissions.
  • Collaborate closely with internal stakeholders.

Kenntnisse

SAS
R
Statistical Analysis
Clinical Research
CDISC Standards

Ausbildung

Bachelor's degree in statistics, biostatistics, mathematics, computer science, or life sciences
Master's in bio/statistics

Jobbeschreibung

On behalf of a renowned client in the life sciences industry, we at Progressive Recruitment are currently looking for a freelance Senior Principal Statistical Programmer (m/f/x) to support an exciting project in the area of Global Medical Affairs.

Your Responsibilities:

  • Conduct statistical analyses for Global Medical Affairs
  • Deliver outputs for publications, abstracts, presentations, conferences, and regulatory/pricing submissions
  • Ensure high-quality and timely delivery in line with Daiichi Sankyo's expectations
  • Collaborate closely with internal stakeholders based on a dynamic publication and submission plan

Your Profile:

  • Bachelor's degree in statistics, biostatistics, mathematics, computer science, or life sciences (Master's in bio/statistics preferred)
  • Experience in clinical research, ideally in drug development or post-marketing (Pharma, CRO, or MedTech)
  • Strong programming skills in SAS and R
  • Solid knowledge of CDISC standards (SDTM, ADaM)
  • Experience with Phase IV studies (interventional and observational), especially in oncology and cardiovascular fields
  • Proven experience in pooling and analyzing multiple databases

Project Details:

  • Start Date: ASAP
  • End Date: 31 March 2026
  • Extension: Possible
  • Workload: 5 days/week (40 hours/week)
  • Location: 100% Remote

Interested?
We look forward to receiving your application!
Please apply with your current CV, including your availability and hourly rate.

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