Clinical Director, Medical Science NMD Pharma A/S
Role highlights
Full Time
Permanent
Lead
On-site
The Clinical Director role at NMD Pharma A/S requires a highly experienced professional with a doctorate-level education (PharmD, PhD, or equivalent) in healthcare or life sciences and at least five years of clinical development experience in biotech or pharmaceutical environments. The candidate must have hands-on expertise in designing and executing phase II and phase III clinical trials, including protocol development, data oversight, and scientific reporting. Strong proficiency in clinical trial methodology, regulatory requirements, and Good Clinical Practice (GCP) standards is essential. The role demands advanced skills in analyzing and interpreting complex clinical data, collaborating with cross-functional teams such as CROs, medical directors, data management, statistics, research, clinical operations, and regulatory affairs. Effective communication in English, both written and oral, is critical for preparing clinical study reports, regulatory documents, scientific publications, and presentations. The position requires autonomous work capability combined with the ability to provide scientific leadership and guidance to ensure scientific integrity and maintain high standards in clinical trial execution and messaging. Experience contributing to clinical development plans and serving as a scientific advisor to multidisciplinary teams is also important. This leadership-level role offers the opportunity to influence clinical development strategies within a dynamic biotech organization focused on advancing phase II programs with precision and scientific rigor.
About the role
- Clinical Director position in the Medical Science team at NMD Pharma A/S
- Reports to Head of Clinical Science
- Location: Aarhus (preferred), Copenhagen, or remote
- Key role in strategic design and execution of clinical development programs
- Ensure scientific integrity and regulatory, scientific, and ethical standards in clinical trials
- Provide cross-functional guidance
Responsibilities
- Lead development of clinical study designs, including protocol writing and related documents
- Plan and review clinical trial data in collaboration with CRO, medical director/monitor, data management, and statistics teams
- Contribute to data analyses, interpretation, and development of Clinical Study Reports, publications, and presentations
- Provide scientific input to regulatory documents and presentations
- Support Medical Science leadership in defining clinical development plans
- Serve as scientific advisor to cross-functional teams (e.g., Research, Clinical Operations, Regulatory)
- Ensure consistency and high standards in scientific messaging and deliverables
Requirements
- PharmD, PhD, or advanced degree in Health Care or relevant life-science discipline
- Minimum 5 years' experience in clinical development within biotech or pharma
- Hands-on experience with data work and scientific oversight
- Experience with phase 2 or phase 3 clinical trials (planning, execution, reporting)
- Strong understanding of clinical trial methodology, regulatory environment, and GCP standards
- Proven ability to analyse and interpret complex clinical data
- Effective communication skills in English (written and oral)
- Ability to work autonomously and collaborate cross-functionally
Benefits
- Join a focused biotech organisation valuing scientific rigour
- Direct influence on clinical development
- Dynamic environment advancing phase II programmes
- Emphasis on precision, clarity, and adaptability
How to Apply
- Submit CV and cover letter via the recruitment portal
- Applications reviewed on an ongoing basis
- For questions, contact Maja Nielsen at [email protected]
- Apply with QuickApply on Jobindex
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