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Open nowPosted 31 days ago

Senior Specialist, Statistical Programming

Pharmacosmos8 open roles

Where
Pharmacosmos A/S, Denmark
Work mode
On site
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Your applicationOpen nowSenior Specialist, Statistical ProgrammingPharmacosmos · Pharmacosmos A/S, Denmark

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The clock on this job

Early applications get read.

12.1% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.1%7 days
  4. 19.1%14 days
  5. 35.6%30 days
  6. 52.7%60 days
This job: posted 31 days ago

The posting

Job description

Join Pharmacosmos and help drive high-quality clinical development through scientific excellence and data-driven decision-making.

We are looking for an experienced Senior Specialist, Statistical Programming to join our Clinical Development team. In this role, you will act as the sponsor-side expert for statistical programming, CDISC standards, and regulatory submissions, ensuring high-quality, compliant, and inspection-ready clinical trial deliverables across our development programs.

Key Responsibilities

  • Provide sponsor oversight and quality review of outsourced statistical programming deliverables.
  • Ensure all datasets and submission deliverables (SDTM, ADaM, Define-XML) meet CDISC standards and regulatory requirements.
  • Contribute to clinical trial documentation, regulatory submissions, and inspection readiness.
  • Perform statistical programming analyses and support data-driven decision-making.
  • Collaborate with cross-functional stakeholders to ensure high-quality clinical trial outputs.
  • Support continuous improvement of programming standards, processes, and best practices.

Qualifications & Experience

  • Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, or a related field.
  • Extensive statistical programming experience within the pharmaceutical or biotechnology industry, ideally 10+ years.
  • Strong expertise in CDISC standards (SDTM, ADaM, Define-XML) and regulatory submissions.
  • Advanced SAS programming skills and a solid understanding of clinical development and regulatory requirements.
  • Experience with R, Python, or other programming languages is considered an advantage.

Personal Competencies You are analytical, detail-oriented, and committed to delivering high-quality results. You work proactively and collaboratively across functions, communicate effectively with stakeholders, and thrive in a dynamic environment where scientific integrity, compliance, and continuous improvement are key.

Why Join Pharmacosmos? At Pharmacosmos, you will become part of an international and purpose-driven organization dedicated to improving patients' lives through innovative treatments. You will work alongside highly skilled colleagues and contribute directly to clinical development programs that make a meaningful difference to patients worldwide.

How to apply You can apply for the position by submitting your application and CV via the "Apply" button above no later than 15 October 2026. Applications will be reviewed on an ongoing basis, and we reserve the right to close the recruitment process once the right candidate has been identified.

For further information about the position, please contact Thomas Delvin, Vice President, Medical Science, at +45 3127 2206 or [email protected].

About Pharmacosmos Pharmacosmos A/S is a global leader in carbohydrate chemistry and innovative treatments for iron deficiency and iron deficiency anaemia. Building on our foundational expertise in carbohydrate chemistry and cell cycle biology, we develop innovative treatments for unmet patient needs, with a focus on iron metabolism and blood-related disorders. Founded in 1965 and headquartered in Denmark, our team is made up of more than 700 specialists across the UK, Ireland, the Nordics, Germany, the USA, and China. Learn more about Pharmacosmos at www.pharmacosmos.com.

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