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Sr Consultant/ Pharmacovigilance System Implementation

年収:800万 ~ 1500万

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部署・役職名 Sr Consultant/ Pharmacovigilance System Implementation
職種
業種
勤務地
仕事内容 Role Definition
Involve in configuration of Pharmacovigilance / Drug Safety Adverse Event Reporting Systems at Pharmaceutical companies which includes understanding Business and Functional requirements, prepare design strategy, develop and implement optimized solutions using prototyping and POC techniques where required.

Job Duties
Key components of the responsibilities are as mentioned below:
• Provide application configuration expertise on Adverse Event Reporting products including, but not limited to Argus Safety, ARISg/j and related modules
• Requirements gathering and analysis
• Development and accountability of document deliverables (Requirement Documents CBD/CS UDDs SCR Verification IQs etc.)
• Design, build and implement configuration for clients
• Conduct POCs to understand the effectiveness of the solution; incorporate feedback into the solution
• Closely work with clients to support implementation and resolve issues
• Implement Quality measures to drive operational efficiencies and articulate the value to the customer
• Closely work with internal teams to support with the implementation and other tasks
• Communicate in both English and Japanese on projects needing bilingual support
応募資格

【必須(MUST)】

• BE/ME/MCA/MCS/MSc degree from reputed Institute/University
• 6-9 years of professional experience and strong knowledge with real time experience in Drug Safety Products from Oracle/Aris Global – Argus/ARISg/j
• Implementation/Upgrade/Maintenance of Drug Safety Application
• Working knowledge of writing SQL queries and/or PL/SQL code
• Experience in handling a team
• Excellent communication and inter-personal skills
• Ability to multi-task and work well under pressure
• Commitment to excellence and high quality standards
• Versatility, flexibility, and a willingness to work within changing priorities
• International travel readiness, work hours that overlap global client location Time-zones
• Business to native level of English and Japanese writing/speaking capability


【歓迎(WANT)】

• Working experience on associated modules like AgExchange/ESM, Percieve, or other Drug Safety Products
• Experience in Customizing E2B profiles
• Experience in configuring Aggregate and Periodic reports
• Knowledge of regulatory guidelines from the Food and Drug Administration (FDA), EMA and PMDA

アピールポイント 外資系企業 女性管理職実績あり 年間休日120日以上 産休・育休取得実績あり 教育・研修制度充実 管理職・マネージャー 完全土日休み フレックスタイム
更新日 2019/09/12
求人番号 1116780

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