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新着求人 プロジェクトマネージャー  (MKI-45)
募集職種 外資系製薬企業の Clinical Scientist, Vaccines
その他のプロジェクトマネージャーの求人はこちら
勤務地 東京
会社概要 非公開
求人要件 The Clinician, Clinical Scientist (CS) will provide leadership in clinical epidemiology study design and execution ensuring consistency of approach, conduct, result reporting and oversight of core team activities within one or more vaccine asset programs.
In collaboration with Clinical Affairs (CA) Biostatistics group and CA Operations the CS is responsible for significant contribution to design, full execution and project management of their studies. Each CS will be responsible for numerous epidemiological studies run either as * sponsored or as Research Collaborations across multiple vaccine products. The Japan CS is a regional position and may support any or all MDSCA projects and Centers of Excellence in Japan or Developed Asia. Post approval commitment studies in China may also be the remit of the Japan CS. The CS will lead via a matrix organization a Core Team for each study requiring collaboration with Epidemiology, Biostats, Clinical Operations, Medical, Regional and * assay group. Data generated by epidemiological studies is critical evidence needed to obtain optimum Vaccine Technical Recommendations at the country level including National Immunization Programs (NIP). Unlike all other TAs, achievement of NIPs is how * drives the vaccines business.
必要要件 •Required: Fluently bi-lingual in English and Japanese
•BA/BS Degree in life sciences or health related field with 8+ years practical experience or MS/MpH with 6+ years.
•Has significant years of strong hands on experience in epidemiology study design, conduct and analysis.
•Has significant experience leading operational and/or strategic study teams
•Has significant experience working independently and collaborating with multiple functional groups within and outside the business line
•Has demonstrated an advanced ability and level of experience with working across multiple studies for incorporation of consistent medical/scientific concepts in multiple protocols and ensuring they meet strategic program objectives
•Has advanced knowledge of the clinical research process and Good Clinical Practices from previous employment experience in the clinical research field
•Has solid knowledge of vaccine therapeutic area
•Has independently authored clinical protocols and other clinical study documents
•Has working knowledge of statistics, data analysis, and data interpretation
•Has experience in managing external vendors for clinical and/or epidemiological studies
•Has exceptional written and oral communication and cross-functional collaborative skills
【PREFERRED QUALIFICATIONS】
•MS or PhD preferred,
•Has experience in working in emerging markets countries
•Is proficient in MS Word, Excel, and Powerpoint
•Prior infectious disease, microbiological or infection control experience
•Has worked in Industry
年収 能力、経験を考慮の上、当社規程により優遇 
募集背景 非公開 
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