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Associate Medical Director GSPV

年収:800万 ~ 1700万

ヘッドハンター案件

部署・役職名 Associate Medical Director GSPV
職種
業種
勤務地
仕事内容 《Primary Function》
The position is responsible for providing safety management, medical oversight and assessment of pharmacovigilance activities as assigned.

《Essential Functions》
•Identifies, communicates and effectively manages potential safety issues

•Works closely with pharmacovigilance colleagues to ensure appropriate medical interpretation and consistency are applied to adverse event case assessment

•Ensures regulatory and SOP compliance with respect to evaluation, reporting and surveillance of clinical safety information

•Provides investigator support regarding safety concerns, medical emergencies, etc

•Participates in medical safety surveillance/signal detection benefit/risk assessment, and development of trend analyses

•Participates in development of REMS and RMP as required

•Discusses and resolves medical issues with clinical sites, clients, and drug safety staff

•Provides medical review and interpretation for aggregate safety reports (e.g. annual safety reports, PSURs, PADERs)

•Consults with internal and external customers in the area of drug safety

•Supports business development through participation in core proposal team activities, feasibility assessments and review of proposals/contracts for medical services

•Maintains medical and pharmacovigilance expertise through appropriate CME


《Supervisory / Management Responsibilities》
•Supervise, coach, and mentor staff

•Oversee development of direct reports by setting goals, conducting performance reviews, evaluating and monitoring training needs, creating development plans, mentoring, and coaching

•Set priorities and schedule activities of departmental resources, implement company objectives, and create alternative solutions to address business and operational challenges
応募資格

【必須(MUST)】

The incumbent should possess M.D., B.M.B.S., D.O. or equivalent degree from an accredited medical school
Minimum of one - two years of experience in clinical practice
•Minimum one year of experience in the pharmaceutical, biotechnology or device industry working in pharmacovigilance/epidemiology
•Knowledge of global pharmacovigilance regulations and processes
•Computer proficient
•Excellent communication, presentation, interpersonal skills, both written and spoken, with an ability to inform, influence, convince, and persuade
•High level of fluency in Japanese language and business level English


給与:前職考慮のうえ決定いたします。
更新日 2018/11/14
求人番号 844264

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