Novartis Group (China) pe jobs (salary & requirements)

The SSO Site Partnership Manager optimizes the cooperation with selected trial sites, considered key accounts fNovartis with huge potential to significantly contribute to the portfolio execution, aiming to improve performance in clinical studies regarding patient numbers, timelines, data flow quality thus establishes Novartis as partner of choice in clinical trials.
Key responsibilities:
In cooperation with study sites:
•Responsible fkey account network within the country/extended country group (OPCs & satellite countries)
•Defines tailored engagement model with assigned sites according to local structural needs of these sites
•Prepares implements Site Partnership Strategy Plans in cooperation with assigned accounts
•Defines measures of success feach site in scope (e.g., % increase in portfolio volume, patient density, start-up, contracting timelines)
•·Single point of contact fall relevant stakeholders (e.g., departments heads, investigators, pharmacists, clinic administration) across all therapeutic areas at assigned sites regarding all study overarching topics
•Communicates Novartis standards & expectations for future collaboration
•Supports feasibility process in close cooperation with Feasibility Manager
•Supports optimizes early site engagement, speed of site initiation readiness as well as achievement of committed patient numbers in the assigned sites
•Responsibility to analyze all information regarding the assigned sites, to oversee all study activities to survey sites´ strengths, areas of improvement capacities
•Support sites in developing network with other departments to improve study start-up, patient management recruitment
•Support negotiation of study fees, contracts, contract templates master templates as applicable
Novartis internal:
•Optimizes Novartis processes to simplify speed up study start-up with focus on site set-up
•Communicates knowledge regarding sites the overarching topics to theganization informs advises relevant functions actively (e. g. site selections)
Essential requirements:
•Degree in scientific health discipline required an advanced degree with clinical trial experience and/project management (preferred)
•Fluent in English local language (written spoken)
•Minimum 5 years’ experience in clinical research in a role that oversees (project management) and/or with monitoring clinical trials
•Capable of leading in a matrix environment, without direct reports
•Understanding of all aspects of clinical drug development with particular emphasis on monitoring study execution
•Strong project management capabilities with demonstrated ability to problem solve mediate complex issues
Desirable requirements:
•Thorough understanding of the international aspects of drug development processes, including strong knowledge of international standards (GCP/ICH), health authorities (FDA/EMA), local/National Health Authorities regulations Novartis standards
•Demonstrated negotiation conflict resolution skills both internal external (site relationships)
•Strong influencing presentation skills
•Strong communication skills
•Communicates effectively in a local/global matrix environment
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职位要求：
VendManagement
Project Planning
Process Improvements
Budget Management
Negotiation
Clinical Trials
Waterfall Model