更新于 2026-05-10 01:14:33
职位描述
肿瘤上市前医学医学监查肿瘤科医生
Essential Functions
● Medical Monitoring:
Primarily serves as Global Medical Advisor on assigned projects.
Serves as Scientific Advisor and provides guidance to Project Leaders on the
medical and scientific aspects of 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.
Performs medical review of the protocol, Investigative Drug Brochure (IDB),
and/or Case Report Forms (CRFs).
Provides therapeutic area/indication training for the project clinical team.
Attends and presents at Investigator Meetings.
Performs review and clarification of trial-related Adverse Events (AEs).
May perform medical case review of Serious Adverse Events (SAEs), including
review of case documentation and patient narrative, in collaboration with the
Pharmacovigilance department.
May provide medical support for the Analysis of Similar Events (AOSE), in
collaboration with or on behalf of Pharmacovigilance department.
May perform medical review of adverse event coding.
Performs review of the Clinical Study Report (CSR) and patient narratives.
Attends Kick-Off meetings, weekly team meetings, and client meetings, as
needed or requested.
Available 24/7 to respond urgent protocol -related questions from
investigative sites, in accordance with local labor laws.
● May require regular travel.
● Extensive use of keyboard requiring repetitive motion of fingers.
● Extensive use of telephone and face-to-face communication requiring accurate
perception of speech.
Qualifications
● Other Medical degree from an accredited and internationally recognized
medical school with a curriculum relevant to general medical education
● Typically requires a minimum of 5-7 years' experience in clinical medicine.
Req: Other Specialty board certification in relevant specialty area preferred.
Req
● Robust and current knowledge of scientific, clinical, regulatory, commercial
and competitive landscape in applicable therapeutic area.
● Knowledge of applicable federal and local regulations and guidelines
pertaining to clinical research.
● Business Acumen
● Other Current or prior license to practice medicine; Clinical experience in
the requested medical specialty. A board-certification for the required
therapeutic area is preferred.
● Medical Monitoring:
Primarily serves as Global Medical Advisor on assigned projects.
Serves as Scientific Advisor and provides guidance to Project Leaders on the
medical and scientific aspects of 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.
Performs medical review of the protocol, Investigative Drug Brochure (IDB),
and/or Case Report Forms (CRFs).
Provides therapeutic area/indication training for the project clinical team.
Attends and presents at Investigator Meetings.
Performs review and clarification of trial-related Adverse Events (AEs).
May perform medical case review of Serious Adverse Events (SAEs), including
review of case documentation and patient narrative, in collaboration with the
Pharmacovigilance department.
May provide medical support for the Analysis of Similar Events (AOSE), in
collaboration with or on behalf of Pharmacovigilance department.
May perform medical review of adverse event coding.
Performs review of the Clinical Study Report (CSR) and patient narratives.
Attends Kick-Off meetings, weekly team meetings, and client meetings, as
needed or requested.
Available 24/7 to respond urgent protocol -related questions from
investigative sites, in accordance with local labor laws.
● May require regular travel.
● Extensive use of keyboard requiring repetitive motion of fingers.
● Extensive use of telephone and face-to-face communication requiring accurate
perception of speech.
Qualifications
● Other Medical degree from an accredited and internationally recognized
medical school with a curriculum relevant to general medical education
● Typically requires a minimum of 5-7 years' experience in clinical medicine.
Req: Other Specialty board certification in relevant specialty area preferred.
Req
● Robust and current knowledge of scientific, clinical, regulatory, commercial
and competitive landscape in applicable therapeutic area.
● Knowledge of applicable federal and local regulations and guidelines
pertaining to clinical research.
● Business Acumen
● Other Current or prior license to practice medicine; Clinical experience in
the requested medical specialty. A board-certification for the required
therapeutic area is preferred.
工作地点
广州越秀区珠江国际大厦
公司信息
艾昆纬医药科技(上海)有限公司
已上市 · 10000人以上 · 医药研发/生产外包（CXO）、互联网医疗、生物/制药
已审核
公司介绍
IQVIA（纽交所代码：IQV）是全球专注生命科学领域的高阶分析、技术解决方案和临床研究服务供应商。IQVIA利用深入分析、前沿技术、大数据资源和广泛领域的专业知识，智能连接医疗生态的各个环节。IQVIA Connected Intelligence™快速敏锐地为客户提供强大的数据洞察，帮助客户加速创新医疗的临床开发和商业化进程，以更好的医疗成果惠及患者。IQVIA拥有约72,000名员工，足迹遍布100多个国家/地区。IQVIA拥有多元化的加强型隐私技术和保障手段，能够在保护个人隐私的同时对信息进行管理和分析，帮助医疗利益相关方有效开展精准疗法，获得更佳的疗效。这些洞见和能力能够帮助生物科技、医疗器械、制药公司、医学研究者、政府机关、支付方以及其他医疗利益相关方，获得对疾病、人类行为和科技进步更深入的理解，共同朝着治愈各类疾病的方向迈进。
工商信息
企业名称 艾昆纬医药科技（上海）有限公司
企业类型 有限责任公司（外国法人独资）
法人代表 BRIAN ZIHOU MI
经营状态 存续
成立时间 2013-07-12
注册资本 200万美元
认证资质
营业执照信息