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
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
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
Job Description Job Title: Senior Director, Regulatory Affairs Strategy - Cell and Gene Therapy Available locations: Barcelona, Spain Amsterdam, Netherlands Introduction to role: Are you ready to set the global regulatory vision for pioneering cell and
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’
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
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has
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
KEY RESPONSIBILITIES Authoring of CMC sections (Drug Product and/or Drug Substance) for new registration applications in CTD format, in alignment with global regulatory strategies and current regulatory guidelines. Authoring and reviewing CMC documentation to support variations and commitments
At ITALFARMACO, we are firmly committed to contributing sustainably to the improvement of peoples health and quality of life. We are an Italian pharmaceutical group with an international presence, dedicated to the research, development, and commercialization
At ITALFARMACO, we are firmly committed to contributing sustainably to the improvement of peoples health and quality of life. We are an Italian pharmaceutical group with an international presence, dedicated to the research, development, and commercialization
At ITALFARMACO, we are firmly committed to contributing sustainably to the improvement of peoples health and quality of life. We are an Italian pharmaceutical group with an international presence, dedicated to the research, development, and commercialization
At ITALFARMACO, we are firmly committed to contributing sustainably to the improvement of peoples health and quality of life. We are an Italian pharmaceutical group with an international presence, dedicated to the research, development, and commercialization
pAt ITALFARMACO, we are firmly committed to contributing sustainably to the improvement of peoples health and quality of life. No deje pasar esta oportunidad, inscríbase rápidamente si su experiencia y habilidades coinciden con lo que se
ALK-Abelló, A/S en Madrid busca un/a Senior Scientist para el grupo de producción, purificación, análisis y control de anticuerpos monoclonales, naturales y recombinantes. Liderará la gestión de prioridades y la documentación de cualificación y verificación en
At ITALFARMACO, we are firmly committed to contributing sustainably to the improvement of peoples health and quality of life. We are an Italian pharmaceutical group with an international presence, dedicated to the research, development, and commercialization
Authoring of CMC sections (Drug Product and/or Drug Substance) for new registration applications in CTD format, in alignment with global regulatory strategies and current regulatory guidelines.Authoring and reviewing CMC documentation to support variations and commitments resulting from interactions
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
At ITALFARMACO, we are firmly committed to contributing sustainably to the improvement of peoples health and quality of life. We are an Italian pharmaceutical group with an international presence, dedicated to the research, development, and commercialization
At ITALFARMACO, we are firmly committed to contributing sustainably to the improvement of peoples health and quality of life. We are an Italian pharmaceutical group with an international presence, dedicated to the research, development, and commercialization