Senior Clinical Scientist — Development & Strategy

Italfarmaco; Alcobendas; Presencial; EUR 55.000 - 75.000; Jornada completa

Descripción de la vacante

Italfarmaco in Madrid is seeking a Clinical Scientist to shape clinical development plans, design protocols, and interpret trial outcomes within a cross-functional team. The role emphasizes scientific excellence and collaboration across Clinical Operations, R&D, Medical Affairs, Regulatory Affairs, and Pharmacovigilance.

You will lead the communication of clinical results, contribute to regulatory submissions, and translate data into strategic insights to guide product development decisions,

Formación

• 5–10+ years of experience in Clinical Science or related roles.
• Experience in clinical development planning and strategy.
• Strong written and oral communication in scientific contexts.

Responsabilidades

• Develop clinical development plans aligned with overall product development strategy.
• Design and develop clinical trial protocols, ensuring scientific rigor, feasibility, and regulatory alignment.
• Provide scientific leadership in planning and design of clinical studies across development phases.
• Review, analyze, and interpret clinical study data for robust efficacy and safety evaluation.
• Critically assess clinical study reports, integrated summaries, and data outputs to support development decisions.
• Contribute to preparation of scientific documentation for regulatory submissions and interactions with health authorities.
• Translate clinical data into strategic insights to support product development decisions.
• Lead dissemination of clinical results, including publications, presentations, and congress abstracts.

Conocimientos

Clinical development

Scientific writing

Regulatory understanding

Cross-functional collaboration

Educación

Scientific degree in Medicine, Pharmacy, Life Sciences, Biotechnology, Biomedical Sciences, or related discipline

Descripción del empleo

Italfarmaco in Madrid is seeking a Clinical Scientist to shape clinical development plans, design protocols, and interpret trial outcomes within a cross-functional team. The role emphasizes scientific excellence and collaboration across Clinical Operations, R&D, Medical Affairs, Regulatory Affairs, and Pharmacovigilance.

You will lead the communication of clinical results, contribute to regulatory submissions, and translate data into strategic insights to guide product development decisions,