Medical Director, Clinical Development (General Clinical Lead)
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Location: Barcelona, Catalonia, Spain
ARTO are partnered with a global Pharmaceutical company, who are committed to the growth of their portoflio within the Medical Dermatology space.
Role Overview
This role provides general medical and scientific leadership for a late-phase clinical development program. The Medical Director (Clinical Lead) will own clinical strategy and execution across Phase II–III studies, acting as the accountable clinical lead within a cross-functional global team and supporting progression toward registration.
Key Responsibilities
- Provide global medical and scientific leadership for a late-phase (Phase II–III) clinical development program, ensuring delivery against quality, timelines, and strategic objectives.
- Define and drive the clinical development strategy, including Target Product Profile (TPP), study concepts, and alignment with regulatory and commercial goals.
- Serve as the clinical lead within global, cross-functional project teams, partnering closely with Clinical Operations, Regulatory Affairs, Safety, Biometrics, and Medical Affairs.
- Act as the medical accountable lead for late-phase clinical studies, including protocol development, data review and interpretation, and ongoing benefit–risk evaluation.
- Represent the clinical program in interactions with external stakeholders, including investigators, key opinion leaders, and regulatory authorities as required.
Candidate Profile & Qualifications
- MD required, with board certification or equivalent clinical training; Dermatology background a strong plus.
- Approximately 5+ years of experience in pharmaceutical or biotechnology clinical development, with exposure to late-phase programs.
- Demonstrated experience contributing at program level within Clinical Development, beyond single-study execution. xsgfvud
- Solid scientific grounding in immunology-driven diseases (e.g. dermatology, allergy, inflammatory or immune-mediated indications).
- Strong understanding of late-phase trial design, clinical data interpretation, and global regulatory expectations.
If you think this role would be a good fit for you, please feel free to reach out to me either through DM, or on email -