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Apply to JobJob ID233623BRPosition TitleBrand Safety LeaderJob DescriptionThe Brand Safety Leader (BSL) serves as scientific safety leader for assigned Novartis projects/products, and, once the project team is formed, is responsible for the integration, analysis, and interpretation of safety information from all sources, including preclinical through lifecycle management (post approval) and externally.



Major accountabilities include:

1. Responsible for safety issue management from end of Phase I (POC) through Life Cycle Management.

2. Responsible for overall signal detection, monitoring, evaluation, interpretation and appropriate management of safety information, based on information from all relevant line functions, postmarketing data, and other sources.

3. Develops and updates, at milestones, the safety profiling and risk management plan from end of Phase I (POC) through Life Cycle Management, as relevant.

4. Leads Safety Management Team. Serves as safety representative on Global Program Teams (extended or core member)

5. Manages Drug Safety Monitoring Board activities for assigned projects/products, as required.

6. Responsible for responses to inquires from regulatory authorities or health care professionals on safety issues. Prepares safety data for health authority review boards. Responsible for re-sponses to legal queries and CPO requests involving safety issues. Ensures safety information communicated to EU Qualified Person in a timely fashion.

7. Provides integrated safety input into all safety relevant parts of regulatory documents (ie IB, CDS, SCS, RMP, CO etc) required during active development, submission phase and during marketing phase.

8. Coordinates involvement of external experts (e.g. authors of “white papers”, members of trial-specific data safety monitoring boards, ad-hoc support for HA meetings, etc.)Minimum requirementsIdeal candidate's background:

• Medical Doctor

• Fluent in spoken and written English.

• 3 years medical experience postdoctoral

• At least 5 years in industry or health authority or CRO (of which 2 years in a global position), including a minimum of 3 years in drug safety

• Experience in preparing clinical safety assessments, risk/benefit evaluations and regulatory reports

•Experience in leading cross-functional, multi-cultural teams

•Experience in preparing RMPs, PSURs, Submission dossiers (SCS).DivisionPHARMABusiness UnitONCOLOGYLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegular

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