- Work under Real-World Evidence team
- Management and implementation of either global or local non-interventional studies (or Phase IV clinical research)
- Project coordinator and key contact of communication between sponsor and investigator
- Conduct site feasibility check, and selection activities for verifying adequate qualifications
- Recruit and select investigators
- IRB and HGRAC preparation, submission and closing; contract preparation and negotiation with research organizations and vendors.
- Monitor investigator performance and adherence to protocols, followed all GCP and GPP procedures and internal SOP
- Data management, to ensure the enrollment process and the quality of data input
- Site initiation and monitoring
- Prepare progress report upon requests and related materials for client meetings
- Manage ongoing studies and maintain good relationship with clients
- Bachelor's degree or above in related discipline, preferably in life science or health-related majors
- More than 2 years experiences in CRA
- Understanding of the Health system policy & management in key global markets, pharmaceutical industry; competitive environment and product development process
- Must work well in a collaborative research environment as well as can work independently with limited supervision
- Enjoy working as part of a team in a fast-paced environment. Excellent time management skills and ability to multi-task and prioritize work.
- Good communication, negotiation and problem-solving skills
- Solid oral and written communication skills in both Chinese and English with ability to describe complex scientific data to a non-technical audience are a must.
- Work under Real-World Evidence team
- Management and implementation of either global or local non-interventional studies (or Phase IV clinical research)
- Project coordinator and key contact of communication between sponsor and investigator
- Conduct site feasibility check, and selection activities for verifying adequate qualifications
- Recruit and select investigators
- IRB and HGRAC preparation, submission and closing; contract preparation and negotiation with research organizations and vendors.
- Monitor investigator performance and adherence to protocols, followed all GCP and GPP procedures and internal SOP
- Data management, to ensure the enrollment process and the quality of data input
- Site initiation and monitoring
- Prepare progress report upon requests and related materials for client meetings
- Manage ongoing studies and maintain good relationship with clients
- Bachelor's degree or above in related discipline, preferably in life science or health-related majors
- More than 2 years experiences in CRA
- Understanding of the Health system policy & management in key global markets, pharmaceutical industry; competitive environment and product development process
- Must work well in a collaborative research environment as well as can work independently with limited supervision
- Enjoy working as part of a team in a fast-paced environment. Excellent time management skills and ability to multi-task and prioritize work.
- Good communication, negotiation and problem-solving skills
- Solid oral and written communication skills in both Chinese and English with ability to describe complex scientific data to a non-technical audience are a must.
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GLG Shanghai, 中国GLG is seeking an Associate to support professional service firm clients. Associates help to drive GLG's business model and develop their segments client base through close coordination with members of the research team and working with clients to fulfill their primary research n ...
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GLG Shanghai, 中国Key Responsibilities · : GLG Associate is responsible for: · Support the client facing team. The Associate will provide project support to the client facing team who manage multiple projects on a day-to-day basis. · Facilitating educational interactions between GLG Network Mem ...
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Third Bridge Shanghai, 中国 全职Job Description · Please note, in applying to this role you are not applying to be a Consultant. Third Bridge is a market-leading investment research firm, we orchestrate and create research for our clients. This role is an Associate in Third Bridge and you'll be working with ou ...
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RWE Clinical Research Associate-Cerner - Shanghai, 中国 - Oracle
描述
Job description:
Qualifications of the ideal candidate:
Job description:
Qualifications of the ideal candidate:
