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Clinical Pharmacology Scientist

NMD Pharma A/S
Aarhus N, København Ø

Locations: Aarhus, Denmark (preferred); Copenhagen, Denmark; or Remote (Europe/US)

Join Us in Transforming Lives Through Innovation

At NMD Pharma, we are committed to delivering life-transforming therapies for people living with neuromuscular diseases. As our new Clinical Pharmacology Scientist, you will play a key role in the clinical development of our innovative drug candidates, from early development phase through late-phase clinical trials ensuring data-driven decision-making to optimize patient outcomes.

This is an exciting opportunity to work in a small, dynamic, and collaborative biotech environment, where your strong scientific capabilities and expertise will have a direct impact on our mission – to develop novel treatments to improve muscle function and quality of life of patients with neuromuscular diseases.

Key Responsibilities:

  • You will be responsible to lead the design and implementation of clinical pharmacology plans in early and late development for the assigned product.
  • You will represent clinical pharmacology in the cross-functional project team for the assigned product, ensuring that clinical pharmacology expertise is applied across the entire drug development, from preclinical through to clinical phases.
  • Design, plan, and oversee clinical pharmacology studies such as human mass balance studies, drug-drug interaction studies and renal/hepatic impairment studies.
  • Support non-clinical development in designing and interpretating PK and TK in non-clinical studies.
  • Analyse and interpret PK and pharmacodynamic (PD) non-clinical data to support dose selection and clinical development strategies for first-in-human studies.
  • Analyse and interpret PK and PD clinical data to support dose selection strategies for late development studies.
  • Lead the development of population PK/PD models in support of clinical development strategies. Support physiologically-based pharmacokinetic (PBPK) modeling for special populations, as required.
  • Contribute to the preparation of clinical pharmacology sections of regulatory documents, including regulatory submissions (IND/NDA/MAA), clinical study protocols, clinical study reports, or investigator brochures.
  • Respond to health authority queries and participate in regulatory meetings, as required.
  • Ensure compliance with global regulatory requirements and industry best practices in clinical pharmacology.

Qualifications:

  • Ph.D., Pharm.D., or M.D. in Pharmacology, Clinical Pharmacology, or a related field.
  • At least 5 years experience in clinical pharmacology within pharmaceutical or biotech industry.
  • Hands-on experience with PK/PD modeling tools, strong analytical skills.
  • Excellent communication and collaboration skills, with a proactive and problem-solving mindset.
  • Up to date with global regulatory guidelines for clinical drug development.

Why Join NMD Pharma?

Impact-driven work. Be part of a team dedicated to improving lives through innovative therapies.

Flexible work options. On-site in Denmark. or remote work (US/Europe)

Collaborative culture. Work in a highly skilled and cross-functional team where ideas turn into action.

At NMD Pharma, we are passionate about our purpose and committed to fostering an inclusive and innovative workplace.

How to Apply

If you are ready to make a difference, we invite you to apply by submitting your application via the QuickApply-button.

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

NMD Pharma is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive work environment.

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