Clinical Research Associate

Primarily responsible for coordinating the various aspects of clinical trials. Works as part of a clinical delivery team providing support, guidance and advice on a local level. Develops existing tools and processes to identify areas of improvement and ensures business continuity for study delivery. Able to solve complex problems within a range of studies.

**Tasks and Responsabilities**
- Identify issues, escalate them and work together with the site to resolve them.
- On-site monitoring in USA.
- Communication with medical researchers.
- Research protocols.
- Conducting clinical studies.
- Regulatory Management.

**Mandatory Requirement**
- Degree in Health Sciences
- 1 - 2 years of experience as CRA
- Advanced English Level
- Visa B1/B2

**Desirable Requirement**
- VEEVA
- English level certification