US-NJ, Associate Global Medical/Scientific Director 235802BR-MZ
Associate Global Medical/Scientific Director
East Hanover, NJ
Research & Development
Medical Affairs support for assigned disease area, compound(s) and/or project(s) under the leadership of the specified disease area Global Group Medical Director. Ensures execution of the medical strategy and tactical plan in regards to specific compound or project.
For assigned compound/indications, work collaboratively across functions and G/R/L, to execute an integrated Medical Affairs plan including clinical trials, publication, medical education and medical information. Collaborates across disease area medical teams. Provides support on Global Medical Affairs clinical trials execution in partnership with global line functions, assigned clinical operations team members, and regional/country medical associates. Provides medical support to CTT s for Novartis sponsored GMA trials. Supports medical training and medical education to internal and external audiences Provides medical support for educational events (e.g. stand-alone meetings, scientific symposia) and scientific congresses within legal and compliance regulations. Provides medical review of key scientific communications, medical information documents and commercial documents within P3 legal and compliance regulations. Provides medical input on overall publication strategy and is a member of publication planning team providing GMA medical input on individual publication plans. Ensures that planning of medical activities and budgets are aligned with global medical affairs processes/standards. Accountable to efficiently manage budgets and resources, including budget planning for future activities. Responsible for developing clinical components of key documents regulatory & safety from GMA studies supporting submissions and post-marketing commitments to health authorities, when applicable.
The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.
MD required for aGMD role, aGSD requires ad-vanced life sciences degree (PharmD, PhD, etc.) Oncology, Hematology, Endocrinology required. Additional business degree is preferred/desired English Proven experience as a successful decisive leader in a strategic multifunctional environment 7 years professional experience within the pharma-ceutical industry, preferably in development and/or medical affairs function at a local, regional or global level. Has developed and implemented global/local Phase II, III or IV trials. Experienced track record of making decisions and aligning the organization behind them. Has good judgement and is a strong decision-maker. Has experience of challenging senior management in relation to science and data. Experience of Medical Expert relationship manage-ment Technical / Functional Skills Has expert operational knowledge and experience in clinical trial design and all stages of clinical trial con-duct (Trial design, Start-up, Execution, Analysis, Re-porting). Has an excellent knowledge of current clinical prac-tice in Oncology/Hematology/Endocrinology or other relevant disease area. Have strong knowledge in and understanding o
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