Sr. Specialist/Ass. Principal Statistical Programmer

Are you passionate about statistical programming? Do you have experience within SAS and CDISC standards?

If so, now is your chance to join Ascendis Pharma as our new Statistical Programmer.

Ascendis Pharma is a fast-growing global biopharmaceutical company committed to making a meaningful difference in patient’s lives. We have locations in Denmark, Germany, the United States, the UK, Italy, Spain, and France.

Guided by our core values of Patients, Science, and Passion, we use our TransCon® drug development platform to fulfill our mission of developing new therapies, selecting only those that demonstrate best-in-class potential to address unmet medical needs.

Today, we are advancing programs in Endocrinology Rare Disease and Oncology. In addition, we collaborate with partners around the world on the development of TransCon-based products for other therapeutic areas and markets.

We seek an experienced Statistical Programmers to strengthen our Statistical Programming team in Hellerup. As a key member of the team, you play a crucial role in:

• Plan, manage, and execute statistical programming activities to support clinical data analysis
• Ensure high-quality deliverables with a strong focus on data integrity and timelines
• Contribute to multi-study analyses and regulatory submissions (e.g., NDA, MAA)
• Promote continual extension and improvement of our programming standards and code libraries
• Coordinate cross-functional operations and deliverables with international colleagues in a dynamic organization

This is an exciting opportunity to work in a fast-paced environment, collaborate with cross-functional, global teams. It offers a unique opportunity to shape the future of a progressive, collegial biometrics unit in Hellerup.

You will be joining the Hub Bravo team consisting of 15 colleagues, and report directly to Claus Stenberg, Associate Director, Head of Statistical Programming Hub Bravo.

Qualifications and Skills:

You hold a relevant academic degree - preferably a Master's or PhD—in statistics, mathematics, computer science, engineering, or life sciences - along with at least ten years of experience in the pharmaceutical, biotechnology, or medical device industry.

Furthermore, you have:

• Proficiency in SAS programming
• Experience with CDISC standards (e.g., SDTM, ADaM) and TFL production
• Experience with regulatory submissions
• Familiarity with R or Python
• Project management experience in programming activities

Key competencies:

You are a strong team player, analytical, and have a can-do attitude.

You possess an entrepreneurial mindset and can thrive in an informal, open environment where innovation and change are key.  

Travel: Up to 20 days per year.

Office: Ascendis Pharma, Tuborg Boulevard 12, 2900 Hellerup

Apply now.

Applications will be evaluated when received, so please apply as soon as possible.

All applications must be submitted in English and are treated confidentially.

For more details about the position or the company, please contact Claus Stenberg csg@ascendispharma.com

You can learn more about Ascendis by visiting our website www.ascendispharma.com

Applications submitted via email or other channels will not be reviewed.