RWE Clinical Research Associate-Cerner
Oracle
- Shanghai
- Permanent
- Full-time
- 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 subject area, 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.
- Which includes being a United States Affirmative Action Employer
- 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 subject area, 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.
- Which includes being a United States Affirmative Action Employer
- Which includes being a United States Affirmative Action Employer