临床研究医师方向
Clinical Research Physician (Pharmaceuticals) – Future Leaders Programme
Education required: PhD degree in clinical medicine.
Language requirement: Written and spoken fluency in your native language and English
Start date: July 2022
Assessment centre dates: April 2022
You’ll be excited by the thought of:
Provide medical input into clinical studies involving China
Asist to develop appropriate protocol synopsis and protocols to support research proposals and meet local registration need
Actively participate feasibilities at program, protocol and site level for global/regional studies, and provide timely and quality feedback
Assist in the medical monitoring and data review for the studies in charge
Prepare and deliver presentations for product and protocol introduction and trainings to study team
Analyze AEs/SAEs, and answer clinical and product queries from investigators
Prepare and finalize local clinical study report under supervisor, and assist study result publication
Provide medical support to deliver regulatory submissions(IND and NDA, etc)
Relevant medical document preparation
Support communication with regulatory agency(including panel meetings, etc) and relevant material preparation
Ensure compliance across all clinical activities
Follow GCP and regulatory guidance
Ensure a high level of self-directed understanding of the GSK
Clinical Research Physician (Pharmaceuticals) – Future Leaders Programme
Education required: PhD degree in clinical medicine.
Language requirement: Written and spoken fluency in your native language and English
Start date: July 2022
Assessment centre dates: April 2022
You’ll be excited by the thought of:
Provide medical input into clinical studies involving China
Asist to develop appropriate protocol synopsis and protocols to support research proposals and meet local registration need
Actively participate feasibilities at program, protocol and site level for global/regional studies, and provide timely and quality feedback
Assist in the medical monitoring and data review for the studies in charge
Prepare and deliver presentations for product and protocol introduction and trainings to study team
Analyze AEs/SAEs, and answer clinical and product queries from investigators
Prepare and finalize local clinical study report under supervisor, and assist study result publication
Provide medical support to deliver regulatory submissions(IND and NDA, etc)
Relevant medical document preparation
Support communication with regulatory agency(including panel meetings, etc) and relevant material preparation
Ensure compliance across all clinical activities
Follow GCP and regulatory guidance
Ensure a high level of self-directed understanding of the GSK
职位类别: 其他
举报温馨提示
- 所属行业:化工、橡胶、玻璃、塑料、涂料、化肥、化纤、石化、助剂、日化、润滑油等
- 所在地区:广西-南宁市
- 联系人:张瑞
- 手机:会员登录后才可查看
- 邮箱:会员登录后才可查看
- 邮政编码:
工作地址
- 地址:






