Clinical Pharmacology Scientist
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 for contributing to the clinical and regulatory development plans and strategies for specific projects. You will collaborate with project teams to implement and execute clinical plans according to applicable guidelines. You will be responsible for the scientific content and strategic fit of clinical pharmacology studies. NMD Pharma works with a fully outsourced operating model utilizing CROs and your ability to lead and oversee complex operations is important.
- Design, plan, and oversee clinical pharmacology studies such as human mass balance studies, drug-drug interaction studies and renal/hepatic impairment studies to assess the pharmacokinetics (PK), and safety of drug candidates.
- Analyse and interpret PK and pharmacodynamic (PD) data to support dose selection and clinical development strategies for first-in-human studies.
- Apply broad clinical pharmacology expertise across the entire drug development value chain, from preclinical through to clinical phases, ensuring smooth transitions and integrated strategies.
- Support non-clinical development in designing and interpretating PK and TK in non-clinical studies
- Collaborate closely with cross-functional teams and experts across the organisation.
- Contribute to the preparation of regulatory documents, including IND/CTA filings, clinical study reports, and investigator brochures.
- 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.
- Expertise in clinical pharmacology, pharmacokinetics, and related areas, across the drug development value chain.
- Strong analytical skills with expertise in PK/PD modelling and simulation including Population PK (PopPK) modelling
- Experience in early-stage pharmacology, including the development and implementation of preclinical pharmacokinetic and pharmacodynamic models.
- 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 this link:
NMD Pharma is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive work environment.
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