年収：1,000万円 〜 1,400万円
|勤務地||東京 / 大阪|
メディカル > CRO・SMO・CMO・CSO
メディカル > 臨床開発・治験関係・CRC・CRA・PV
Medical Monitoring: primarily acts as back-up Medical Advisor but may serve as Regional Medical Advisor on assigned projects. Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications, inclusion/exclusion determinations, and issues of patient safety and/or eligibility. May contribute to the medical review of the protocol, Investigative Drug Brochure (IDB) and/or Case Report Forms (CRFs). Performs review and clarification of trial-related Adverse Events (AEs). May perform medical case review of Serious Adverse Events (SAEs). May provide medical support for the Analysis of Similar Events (AOSE), in collaboration with or on behalf of Pharmacovigilance department. Performs review of the Clinical Study Report (CSR) and patient narratives. vailable 24 hours per day, 7 days per week to respond to urgent protocol-related issues at the investigative sites.
泌尿器癌専門医&血液癌専門医 MD licence（医師免許必須） Clinical Experience in Oncology-Urology in Japan Current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in applicable therapeutic area. Good communication, presentation and interpersonal skills, including good command of English language (both written and spoken). Ability to establish and maintain effective working relationships with coworkers, managers and clients. Attention to details, ability to provide advice on multiple assignments and flexibility.