Design Head

Jordan martorell s.l.; Sant Vicenç dels Horts; Presencial; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

A medical device company in Sant Vicenç dels Horts is seeking a Head of Clinical Evaluation. You will oversee the development of clinical documentation and conduct systematic literature reviews. The ideal candidate has strong writing expertise and is bilingual in English and Spanish. This role offers a permanent contract with flexible working hours for a healthy work-life balance.

Servicios

Permanent and stable contract

Professional development opportunities

Flexible working hours

Formación

• Experience in writing and validating clinical documentation.
• Expert in conducting systematic literature reviews.
• Bilingual in English and Spanish.

Responsabilidades

• Oversee key clinical documentation development.
• Execute systematic literature reviews with traceability.
• Prepare and approve Clinical Evaluation Reports.

Conocimientos

Strong expertise writing

Literature appraisal

Systematic literature searches

Familiarity with reference management tools

Descripción del empleo

Overview

At iVascular , we are dedicated to the design, manufacturing, production, and commercialization of medical devices for the treatment of cardio, neuro, and endovascular diseases and to become a reference in the vascular field by enhancing the value of technology and innovation. We are a national company founded in 2010 in Barcelona (Spain) in a phase of growth and international expansion, with subsidiaries already established in Europe, Latin America, Canada, and China, and a team of more than 550 employees covering the entire manufacturing process through vertical integration.

Responsibilities

We are currently seeking a passionate and experienced Head of Clinical Evaluation to join our Clinical team at our site in Sant Vicenç dels Horts (Barcelona). You will oversee the development, writing and supervision of all key clinical documentation, ensuring high-quality systematic literature reviews and the preparation, review and approval of Clinical Evaluation Reports, always in full compliance with the European Medical Device Regulation.

Oversee and execute comprehensive systematic literature reviews, ensuring robust methodology, full traceability and the appropriate use of specialized databases. Critically appraise all available clinical evidence—both internal data and published literature—to support well-founded conclusions on device safety and performance. Direct and contribute to the development, writing, validation and approval of Literature Search Reports and Clinical Evaluation Reports (CERs). High level of English and Spanish.

Qualifications

• Strong expertise writing, literature appraisal and systematic literature searches.
• Familiarity with reference management tools (Zotero, Mendeley, etc.).

Benefits

Permanent and stable contract in a project with high global impact and expanding internationally. Professional and personal development in a vibrant, dynamic, and youthful environment. Flexible working hours to support a healthy work-life balance.