Associate Director Regulatory Affairs
Vor 2 Tagen
As a leader in the pharmaceutical industry, Novartis seeks a highly skilled Biomedical Research Submission Management, Associate Director to join our team. This individual will be responsible for leading cross-functional submission sub-teams to project manage regulatory submissions.
About the Role- Manage local submission management teams.
- Prepare BR submission components including NDA and MAA dossiers.
- Develop strategic submission plans and execute them.
- Provide data visuals and monitor critical path activities.
- Manage local submission management team.
- Oversee preparation of BR submission components including NDA and MAA dossiers.
- Lead submission planning discussions and develop comprehensive strategic submission plan.
- Monitor progress and provide updates to stakeholders.
- Competitive compensation package.
- Opportunities for professional growth and development.
- Inclusive work environment.
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Basel, Basel-Stadt, Schweiz Novartis Farmacéutica VollzeitJob DescriptionWe are looking for a highly experienced professional to lead our Biomedical Research Submission Management team as an Associate Director at Novartis Farmacéutica.This role involves managing the preparation of regulatory submissions, including NDA and MAA dossiers, ensuring compliance with relevant regulations and company standards.Manage...
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