About Ardena Ardena is a global Contract Development and Manufacturing Organization (CDMO) and Contract Research Organization (CRO) specializing in precision medicine development. Ardena supports pharmaceutical and biotechnology companies in bringing innovative, complex molecules from discovery to market. The
1. Job Title: Director of Clinical Pharmacology and Quantitative Pharmacology 2. Introduction to role: Are you ready to lead model-informed drug development that shapes dose strategy from first-in-human through registration? In this Barcelona-based leadership role, you will
1. Job Title: Director of Clinical Pharmacology and Quantitative Pharmacology 2. Introduction to role: Are you ready to lead model-informed drug development that shapes dose strategy from first-in-human through registration? In this Barcelona-based leadership role, you will
Location: Barcelona - Spain (3 days working from the office and 2 days working from home) Introduction to the role The RAD provides strategic and operational regulatory leadership to the development, commercialisation and life cycle management of
How You’ll Make an Impact: The Director, Clinical Development – EMEAI serves as the senior regional Clinical Development leader and primary clinical liaison for the EMEAI region. This role supports global clinical development programs across primarily pharmaceutical products, with
Regulatory Consultant – CMC (small molecule products) Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them
Regulatory Consultant - CMC (CMC with small molecule products) Envíe su CV y cualquier información adicional requerida después de haber leído esta descripción, haciendo clic en el botón de solicitud. Syneos Health® is a leading fully-integrated life sciences
Regulatory Consultant – CMC (small molecule products) Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them
We’re looking for a Senior Software Engineer - AI Product development to join our Cortellis CMC team in Barcelona , where you’ll work on high-impact backend services that power global pharmaceutical innovation. In this role, you’ll take strong
Presente su candidatura después de leer los siguientes requisitos de habilidades y cualificaciones para este puesto. Oxford Global Resources is seeking a Global CMC Regulatory Affairs Manager Consultant to support as external contractor on behalf of Oxford
Regulatory Consultant - CMC (CMC with small molecule products) Usted podría ser el solicitante perfecto para este trabajo. Lea toda la información asociada y asegúrese de presentar su candidatura. Updated: Yesterday Location: Madrid, Spain Job ID: -OTHLOC-3529-2DMAD-2DR Description
Description Regulatory Consultant - CMC (CMC with small molecule products) Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum,
Regulatory Consultant - CMC (CMC with small molecule products) Usted podría ser el solicitante perfecto para este trabajo. Lea toda la información asociada y asegúrese de presentar su candidatura. Updated: Yesterday Location: Madrid, Spain Job ID: -OTHLOC-3529-2DMAD-2DR Description
Regulatory Consultant - CMC (CMC with small molecule products) Envíe su CV y cualquier información adicional requerida después de haber leído esta descripción, haciendo clic en el botón de solicitud. Syneos Health® is a leading fully-integrated life sciences
Company name: ONA Therapeutics Para una comprensión completa de esta oportunidad y de lo que se requerirá para ser un candidato exitoso, siga leyendo. Job location: Barcelona, Catalonia, Spain (On-site, hybrid, or remote) Reporting line: C-level
In a nutshell Position: Regulatory Affairs Manager - Biosimilars Location: Madrid (on-site) Experience: 5+ years in Regulatory Affairs within biotech/biopharma Want to know more? INSUD PHARMA operates across the entire pharmaceutical value chain, bringing specialist knowledge
We’re building the future of medical dermatology by focusing on unmet patient needs and giving people the space to think independently, take ownership and make an impact that matters.Our purpose is simple: to transform patients’ lives
Description Senior Medical Editor. FSP Spain. Must have previous clinical editing exp. Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the
Job Title Director of Clinical Pharmacology and Quantitative Pharmacology Introduction to Role Are you ready to lead model-informed drug development that shapes dose strategy from first‑in‑human through registration? In this Barcelona‑based leadership role, you will guide the
McDermott Laboratories Limited Aunque la experiencia profesional y las cualificaciones son clave para este puesto, asegúrese de comprobar si posee las habilidades interpersonales preferibles antes de solicitar, si se requieren. Key responsibilities for this role include: