Clinical Director, Medical Science NMD Pharma A/S
Role highlights
Full Time
Permanent
Lead
On-site
The Clinical Director, Medical Science role at NMD Pharma A/S requires an advanced degree such as a PharmD, PhD, or equivalent in healthcare or life sciences, reflecting a high level of academic rigor. Candidates must have a minimum of five years of hands-on experience in clinical development within the biotech or pharmaceutical industry, with a focus on phase II and phase III clinical trials. Key competencies include strategic clinical study design, protocol development, and oversight of clinical trial execution, ensuring adherence to regulatory, scientific, and ethical standards including Good Clinical Practice (GCP). The role demands expertise in collaborating with cross-functional teams such as CROs, medical directors, data management, and biostatistics to plan, review, and interpret complex clinical data. Strong skills in data analysis, clinical study reporting, and contributing to regulatory documentation and scientific publications are essential. Effective communication skills in English, both written and oral, are required to provide scientific guidance and maintain consistency in messaging across diverse teams. The candidate should demonstrate autonomy in driving clinical development plans while fostering collaboration to support organizational goals. This leadership position emphasizes scientific integrity, precision, and adaptability within a dynamic biotech environment focused on advancing phase II programs. Overall, the role suits a seasoned clinical development professional with proven ability to lead clinical science initiatives, apply rigorous methodology, and influence clinical strategy in a regulated, multidisciplinary setting.
About the role
Role Summary
- Join the Medical Science team as Clinical Director
- Report to the 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, 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 of experience in clinical development within biotech or pharma
- Hands-on experience with data work and scientific oversight
- Experience in 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, both written and oral
- Ability to work autonomously and collaborate cross-functionally
Benefits
- Join a focused biotech organisation valuing scientific rigour
- Directly influence clinical development
- Be part of a dynamic environment advancing phase II programmes
- Work in a setting that demands precision, clarity, and adaptability
How to Apply
- Submit your CV and cover letter via the recruitment portal
- Applications reviewed on an ongoing basis
- Apply with QuickApply on Jobindex
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