Associate Manager, Site Quality & Compliance
Boehringer Ingelheim View all jobs
- Shanghai
- Permanent
- Full-time
- As a member of Clinical Development & Operations(CDO) Site Quality & Compliance, be responsible for the site quality and compliance initiatives in assigned area, this will include but not limited to:
- Implement global and local site quality and compliance initiatives
- Participate, support and actively contributes to continuous process improvements, knowledge management and training management within CDO, when applicable
- Work closely with Quality Medicine(QM) team to identify areas for site quality and compliance improvement and discuss suggestions; support CDO to plan /strategize site quality and compliance initiatives and ensure implementation
- Inspection and audit readiness
- Work with QM and other stakeholders in Medicine to support CTMs and CRAs during a site inspection or sponsor inspection; furthermore, coordinate certain activities on behalf of clinical operations, if required and appropriate.
- Minimum 5 years' experience in clinical operations, including at least 1 year quality relevant experience and experience with inspection and audit
- Project management experience or equivalence will be a plus
- Excellent understanding of ICH GCP, and other applicable regulations, policies related to clinical trials
- Strong Quality sense and proven records of high quality standard
- Good communication and organization skills
- Fluent in reading, writing and speaking English