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Director Global Regulatory Affairs (Oncology)(m/w/x)
Defining regulatory strategy for antibody/ADC cancer therapies, including novel combination and companion diagnostics, at biotech firm. 9+ years experience with antibody/ADC cancer therapy regulatory processes required. Directing global market authorization for novel cancer therapies.
Requirements
- University degree in natural sciences or equivalent
- 9+ years of working experience in Regulatory Affairs
- Experience in development of antibody- and ADC-based cancer therapies
- Experience in novel combination therapy and companion diagnostic development
- Team-oriented and solution-oriented mindset
- Experience in regulatory strategy planning
- Proven ability to plan, coordinate and lead activities
- Knowledge of multidisciplinary functions in drug development
- Business fluent English
Tasks
- Act as Global Regulatory Lead for assigned development projects
- Define and execute the Regulatory Strategy from clinical development to marketing authorization
- Plan, prepare, and conduct interactions with national and supranational authorities
- Define the strategy for regulatory interactions for assigned projects
- Develop the storyline for regulatory applications and dossiers
- Coordinate the preparation, writing, and reviewing of regulatory documents
- Contribute to the setup and optimization of regulatory processes and systems
- Represent Global Regulatory Affairs in cross-functional initiatives
- Supervise vendors involved in regulatory affairs
- Monitor changes in the regulatory landscape and analyze their impact
- Build transparent relationships with regulatory agencies for assigned projects
Work Experience
- 9 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Not a perfect match?
- Boehringer IngelheimFull-timeOn-siteSeniorIngelheim am Rhein
- BioNTech SE
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Director Global Regulatory Affairs (Oncology)(m/w/x)
Defining regulatory strategy for antibody/ADC cancer therapies, including novel combination and companion diagnostics, at biotech firm. 9+ years experience with antibody/ADC cancer therapy regulatory processes required. Directing global market authorization for novel cancer therapies.
Requirements
- University degree in natural sciences or equivalent
- 9+ years of working experience in Regulatory Affairs
- Experience in development of antibody- and ADC-based cancer therapies
- Experience in novel combination therapy and companion diagnostic development
- Team-oriented and solution-oriented mindset
- Experience in regulatory strategy planning
- Proven ability to plan, coordinate and lead activities
- Knowledge of multidisciplinary functions in drug development
- Business fluent English
Tasks
- Act as Global Regulatory Lead for assigned development projects
- Define and execute the Regulatory Strategy from clinical development to marketing authorization
- Plan, prepare, and conduct interactions with national and supranational authorities
- Define the strategy for regulatory interactions for assigned projects
- Develop the storyline for regulatory applications and dossiers
- Coordinate the preparation, writing, and reviewing of regulatory documents
- Contribute to the setup and optimization of regulatory processes and systems
- Represent Global Regulatory Affairs in cross-functional initiatives
- Supervise vendors involved in regulatory affairs
- Monitor changes in the regulatory landscape and analyze their impact
- Build transparent relationships with regulatory agencies for assigned projects
Work Experience
- 9 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
About the Company
BioNTech SE
Industry
Pharmaceuticals
Description
Das Unternehmen entwickelt bahnbrechende Medikamente zur Verbesserung der globalen Gesundheit und zur Bekämpfung von Krankheiten.
Not a perfect match?
- Boehringer Ingelheim
Global Regulatory Strategy Lead(m/w/x)
Full-timeOn-siteSeniorIngelheim am Rhein - BioNTech SE
(Senior-) Director Clinical Development(m/w/x)
Full-timeOn-siteSeniorMainz, München - BioNTech SE
Director Clinical Operations(m/w/x)
Full-timeOn-siteSeniorMainz - BioNTech SE
Director Translational Sciences (Oncology)(m/w/x)
Full-timeOn-siteSeniorMainz - BioNTech SE
Director AS&T Projects & Strategy(m/w/x)
Full-timeOn-siteSeniorMainz