社名
社名非公開
職種
メディカルアフェアーズ、学術
業務内容
...
■Major Responsibilities:●Develop and maintain in depth knowledge for assigned product(s) / relevant therapeutic area(s) through attendance / participation at key internal meetings/training sessions, relevant congresses, and seminars and by regular self-study of the national/international literature.●Provide expert medical advice for assigned products and related therapeutic areas, including responding to requests for scientific/technical information; contribute to the development, medical and scientific accuracy of core dossiers generated by the medical department.●Establish and maintain professional and credible relationships with external experts and academic centers; this will involve participating in scientific congresses, coordinating advisory boards, round-table meetings, discussion forums, etc.●Deliver scientific presentations and medical education programs to healthcare professionals individually or in groups (meetings, clinical sessions, etc.), where requested. Develop and update medical education materials.●Screen relevant literature and other information from relevant scientific societies meetings and conferences and develop summaries of key messages for use within the Company (e.g. key areas of scientific/company interest, new trends in diagnosis, monitoring and treatments in the therapeutic area, etc.)●Contribute medically to the training for sales forces and other departments; develop and update relevant training materials.●Medical Research Activities:Design and implement Medical research projects within defined standards and budgets (e.g. Phase IV, post marketing clinical activities such as registry/database projects, epidemiological surveys, and PMOS studies).●Provide the required oversight to manage review, approval and conduct of IIS studies.●Support the affiliate Clinical Research Department in the management of clinical studies, as appropriate (e.g. review new clinical study protocols, identifying potential investigators/sites
求められる経験
●Medical Doctorate (M.D.) and Ph.D. in Oncology with relevant therapeutic specialty in an
academic or hospital environment. Completion of residency and/or fellowship is preferred.
● Minimum of 2 years of clinical trial or medical affairs experience in the pharmaceutical industry or academia or equivalent. 3+ years of experience is preferred.
● Knowledge of clinical trial methodology, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols.
● Must possess excellent oral and written English communication skills.
保険
健康保険,厚生年金保険,雇用保険
休日休暇
日曜日,土曜日,祝日
給与
年収1,000 ～ 1,600万円
賞与
-
show more
社名
社名非公開
職種
メディカルアフェアーズ、学術
業務内容
■Major Responsibilities:●Develop and maintain in depth knowledge for assigned product(s) / relevant therapeutic area(s) through attendance / participation at key internal meetings/training sessions, relevant congresses, and seminars and by regular self-study of the national/international literature.●Provide expert medical advice for assigned products and related therapeutic areas, including responding to requests for scientific/technical information; contribute to the development, medical and scientific accuracy of core dossiers generated by the medical department.●Establish and maintain professional and credible relationships with external experts and academic centers; this will involve participating in scientific congresses, coordinating advisory boards, round-table meetings, discussion forums, etc.●Deliver scientific presentations and medical education programs to healthcare professionals individually or in groups (meetings, clinical sessions, etc.), where requested. Develop and update medical education materials.●Screen relevant literature and other information from relevant scientific societies meetings and conferences and develop summaries of key messages for use within the Company (e.g. key areas of scientific/company interest, new trends in diagnosis, monitoring and treatments in the therapeutic area, etc.)●Contribute medically to the training for sales forces and other departments; develop and update relevant training materials.●Medical Research Activities:Design and implement Medical research projects within defined standards and budgets (e.g. Phase IV, post marketing clinical activities such as registry/database projects, epidemiological surveys, and PMOS studies).●Provide the required oversight to manage review, approval and conduct of IIS studies.●Support the affiliate Clinical Research Department in the management of clinical studies, as appropriate (e.g. review new clinical study protocols, identifying potential investigators/sites
...
求められる経験
●Medical Doctorate (M.D.) and Ph.D. in Oncology with relevant therapeutic specialty in an
academic or hospital environment. Completion of residency and/or fellowship is preferred.
● Minimum of 2 years of clinical trial or medical affairs experience in the pharmaceutical industry or academia or equivalent. 3+ years of experience is preferred.
● Knowledge of clinical trial methodology, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols.
● Must possess excellent oral and written English communication skills.
保険
健康保険,厚生年金保険,雇用保険
休日休暇
日曜日,土曜日,祝日
給与
年収1,000 ～ 1,600万円
賞与
-
show more
