The role is accountable for performance and compliance for assigned protocols and sites in a country under the oversight of the Clinical Research Associate manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our company policies and procedures, quality standards and adverse event reporting requirements internally and externally.
Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation.
Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine.
**Responsibilities**:
- Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.
- Actively develops and expands the territory for clinical research, finding and developing new sites.
- Participates in internal meetings and ...