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Clinical Director, Medical Science NMD Pharma A/S

NMD Pharma A/S
Aarhus, Copenhagen or Hybrid

We are seeking a Clinical Director to join our Medical Science team. The role reports to the Head of Clinical Science, and will be based in Aarhus (preferred), Copenhagen, or remote. You will play a key part in the strategic design of our clinical development program, ensure adequate planning and execution of the clinical programs, the scientific integrity of our clinical data, as well as providing guidance across functions. In this role, you will ensure that clinical trials meet regulatory, scientific, and ethical standards.

Key responsibilities

  • Lead in the development of clinical study designs, including protocol writing, amendments, ICFs and other protocol related documents.
  • Plan and conduct ongoing review of clinical trial data of the assigned studies in close collaboration with the assigned CRO, the medical director or medical monitor, data management and the statistics teams to ensure adequate data quality in support of the analysis of clinical trial results.
  • Provide input into data analyses and interpretation including the development of the Clinical Study Report, publications and internal/external presentations.
  • Provide scientific contribution to regulatory documents, publications and presentations.
  • Support the Medical Science leadership in defining clinical development plans.
  • Serve as scientific advisor to cross-functional teams (e.g., Research, Clinical Operations, Regulatory).
  • Ensure consistency of scientific messaging across internal and external materials, and maintain high standard in all deliverables.

Your qualifications

  • PharmD, PhD or advanced degree in Health Care or in a relevant life-science discipline.
  • At least 5 years of experience in clinical development within biotech or pharma, with hands-on data work and scientific oversight.
  • Experience in conducting phase 2 or phase 3 clinical trials including planning, executing, and/or reporting.
  • Strong understanding of clinical trial methodology, regulatory environment and GCP standards.
  • Proven capability to analyse and interpret complex clinical data sets. Ability to communicate scientific content effectively in English, both written and oral.
  • Capacity to work autonomously, while actively participating in team decisions and cross-functional collaboration.

What we offer

You will join a focused biotech organisation where scientific rigour is highly valued and where your contributions will directly influence clinical development. As we advance our phase II programmes, you will be part of a dynamic environment that demands precision, clarity and adaptability.

How to apply

Please submit your CV and cover letter via our recruitment portal. Applications will be reviewed on an ongoing basis.

If you have questions regarding the position, please contact Maja Nielsen – mbn@nmdpharma.com.

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