Descripción de la oferta
Medical Director, Clinical Development (Global Clinical Lead)
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ARTO is partnered with a global Pharmaceutical company, committed to the growth of its portfolio within the Medical Dermatology space.
This role provides global 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.
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.
Qualifications
MD required, with board certification or equivalent clinical training.
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.
Strong understanding of late‑phase trial design, clinical data interpretation, and global regulatory expectations.
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