Statistican

Are you excited by working with clinical trial data and influencing trial design and methodology? Do you enjoy taking ownership, collaborating across functions, and contributing to high‑quality clinical development? If so, you may be our new Statistician. Position Overview In this role, you will be the statistician responsible for individual clinical trial(s) and contribute to regulatory submissions and regulatory requests. As a cross‑functional trial team member, you will represent Biostatistics and act as the main point of contact on all trial related aspects. Responsibilities Ensuring fit‑for‑purpose trial design, methodology, and statistical quality, and leading biostatistical discussions within the trial team Contributing to the authoring and review of trial outlines, protocols, statistical analysis plans (SAPs), and statistical sections of clinical study reports, including deliverables from CROs Collaborating closely with internal trial teams and CROs to ensure timely and high‑quality deliverables Driving the evaluation and interpretation of clinical trial data, and preparing and presenting key results at internal decision‑making forums Perform statistical analysis to understand individual trial results and support regulatory interactions or scientific publications Qualifications Master’s degree or PhD in statistics or mathematics At least 2 years of experience within clinical development Experience with trial outline, protocol, SAP, statistical analysis of clinical trials or clinical trial reporting authoring Previous experience working with SAS or R and knowledge of CDISC data model Experience working with CROs and outsourced clinical trial activities (an advantage) Experience with early phase trials (an advantage) The ability to act as a subject‑matter expert within your area and work independently in teams with stakeholders outside Biometrics, with the possibility of sparring with more senior colleagues Adaptable to changing priorities Job Details Seniority level: Entry level Employment type: Full‑time Job function: Research, Analyst, and Information Technology Your new team You will join the Biostatistics Department, part of the Biometrics function alongside Data Management and Statistical Programming. Biometrics plays a central role in shaping the clinical development strategy for Zealand’s compounds, ensuring scientific rigor across development programs and interactions with regulatory authorities. Culture We have a unique culture, characterized by excellent teamwork and strong engagement across the organization. We bond through curiosity and playfulness as a team, allowing ourselves to challenge common thinking and drive future innovation. Join us and let’s bond and be bold. Application Process Interested in bonding with us? Apply no later than January 14, 2026 or as soon as possible. The applications will be reviewed as they come in. While a cover letter is not required, please include a few sentences in your CV explaining your motivation for applying. Contact For further information, please contact VP, Biometrics, Per Sørensen at . Equal Opportunity Employer We are committed to an inclusive recruitment process and welcome applications from all job applicants. About Zealand Pharma A/S Zealand Pharma A/S (Nasdaq: ZEAL) is a biotechnology company focused on the discovery and development of peptide‑based medicines. More than 10 drug candidates invented by Zealand Pharma have advanced into clinical development, of which two have reached the market and three candidates are in late‑stage development. The company has development partnerships with a number of pharma companies as well as commercial partnerships for its marketed products. Zealand Pharma was founded in 1998 and is headquartered in Copenhagen, Denmark, with a team in the U.S. For more information about Zealand Pharma’s business and activities, please visit . #J-18808-Ljbffr