Drug Safety Associate
上海任仕达人才服务有限公司
- 公司规模：150-500人
- 公司性质：外资(欧美)
- 公司行业：专业服务(咨询、人力资源、财会)
职位信息
- 发布日期：2013-01-15
- 工作地点：上海
- 招聘人数：若干
- 工作经验：三年以上
- 学历要求：本科
- 语言要求：英语熟练
- 职位类别：生物工程/生物制药
职位描述
Location: China-Shanghai
l A global leading healthcare company from UK
l Committed to finding talent, ideas and new medicines in internal Research and Development (R&D) community
l Worldwide Business Development group is a global team of scientific
Key responsibilities:
l Collection of adverse events (AEs), recording in the country register and reporting of AEs to Central Safety Depts
l Keep contact with GCSP/CR team/Inv./EC/SFDA to make sure safety system work well and compliance with relevant SOPs/Regulations/GCP
l Submission of PSURs and other periodic safety updates to Regulatory Authorities, Investigators and Ethics Committees as required.
l Review Protocol/CRF/CSR of local sponsored study and CSP of GSK Supported Study to make sure relevant content is compliance with SOPs/Regulations/GCP
l Provide drug safety related training to GSK China personnel (sales and CRA, particular)
l Deal with compensation
l Responsible for safety SOP update and LOCALE administration
Qualifications required
l Medical bachelor degree or above
l Previous experience in clinical medicine
l Better have pharmacovigilance related working experience
l Good at team work and English
Benefit:
l World-class training and developing courses
l Promotion plan for every year
l Competitive salary and bonus system
If you're interested, please contact me
May.wang@randstad.cn. If you want to look for other opportunity, also you can go to our website: www.randstad.com
l A global leading healthcare company from UK
l Committed to finding talent, ideas and new medicines in internal Research and Development (R&D) community
l Worldwide Business Development group is a global team of scientific
Key responsibilities:
l Collection of adverse events (AEs), recording in the country register and reporting of AEs to Central Safety Depts
l Keep contact with GCSP/CR team/Inv./EC/SFDA to make sure safety system work well and compliance with relevant SOPs/Regulations/GCP
l Submission of PSURs and other periodic safety updates to Regulatory Authorities, Investigators and Ethics Committees as required.
l Review Protocol/CRF/CSR of local sponsored study and CSP of GSK Supported Study to make sure relevant content is compliance with SOPs/Regulations/GCP
l Provide drug safety related training to GSK China personnel (sales and CRA, particular)
l Deal with compensation
l Responsible for safety SOP update and LOCALE administration
Qualifications required
l Medical bachelor degree or above
l Previous experience in clinical medicine
l Better have pharmacovigilance related working experience
l Good at team work and English
Benefit:
l World-class training and developing courses
l Promotion plan for every year
l Competitive salary and bonus system
If you're interested, please contact me
May.wang@randstad.cn. If you want to look for other opportunity, also you can go to our website: www.randstad.com
公司介绍
Randstad is the world’s second largest HR services organisation and widely recognised as a global Fortune500 company. Commencing operations in Amsterdam in the 1960s, our international branch network of 4700 offices now extends across 40+ countries worldwide and we employee a team of more than 27,000 professional consultants.
Randstad China first opened offices in 2005 and we have an established branch network across China, servicing more than 100 primary and secondary cities. With a focus on rapid expansion over the next three years, we now look to accelerate our business by investing in the growth and development of our team in Shanghai.
Randstad China first opened offices in 2005 and we have an established branch network across China, servicing more than 100 primary and secondary cities. With a focus on rapid expansion over the next three years, we now look to accelerate our business by investing in the growth and development of our team in Shanghai.