Job Description
**Clinical Research Associate - São Paulo Brazil**
**(Level Depending on Experience)**
**Job Purpose/Summary**
Completes project activities associated with monitoring functions of Phase I through Phase IV clinical research studies while continuing to develop knowledge of drug development process, ICH / Good Clinical Practice (GCP), and applicable local regulations. Provides clinical and technical support for Clinical Research Associates (CRAs) and administrative staff. Performs management of study site activities to ensure integrity of clinical data in adherence to all applicable regulatory guidelines and Standard Operating Procedures (SOPs).
**What You'll Do**
- Manages investigative site activity for multiple protocols / indications and provides ongoing updates of site status to Study Manager / sponsor.
- Conducts study site visits (pre-study, initiation, monitoring, and close-out) and completes site visit deliverables within given timelines in the Monitoring Plan.<...
**(Level Depending on Experience)**
**Job Purpose/Summary**
Completes project activities associated with monitoring functions of Phase I through Phase IV clinical research studies while continuing to develop knowledge of drug development process, ICH / Good Clinical Practice (GCP), and applicable local regulations. Provides clinical and technical support for Clinical Research Associates (CRAs) and administrative staff. Performs management of study site activities to ensure integrity of clinical data in adherence to all applicable regulatory guidelines and Standard Operating Procedures (SOPs).
**What You'll Do**
- Manages investigative site activity for multiple protocols / indications and provides ongoing updates of site status to Study Manager / sponsor.
- Conducts study site visits (pre-study, initiation, monitoring, and close-out) and completes site visit deliverables within given timelines in the Monitoring Plan.<...