A fast-growing international pharmaceutical services company is looking for professional enthusiastic candidates to fill a full-time position of a Clinical Research Associate in Ecuador for monitoring, on-site quality control of multi-center international clinical trials of novel pharmaceuticals; including also the preparation, conduct and reporting of routine, start up, close out monitoring visits and other tasks related to communication, quality control, training, quality assurance, data management, regulatory affairs, document and site management.
We require:
• Prior clinical research experience as CRA/monitor (at least 1 year).
. Higher medical education (MD) or degree in life sciences;
• Fluent English, both spoken and written;
• Desire and ability to learn fast, work hard and travel up to 80% of the time;

A successful candidate will also be computer literate, hard-working, result-oriented, and have problem solving expertise, should be flexible and willing to take on challenging tasks in a fast-paced and energetic working environment.
We offer competitive employment, extensive training and good opportunities for personal and professional growth.
To apply, please Email your CV in English (with ref: CRA) at
xxx@xxx-xxx.xxx