**Clinical Research Associate**

**Your responsibilities will include:**

+ Performing site selection, initiation, monitoring and close-out visits
+ Supporting the development of a subject recruitment plan
+ Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines
+ Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
+ Collaborating with experts at study sites and with client representatives

**Qualifications:**

+ University degree in scientific discipline or health care
+ 2-4 years of independent on-site monitoring experience.
+ Very good computer skills including MS Office
+ Excellent command of Portuguese and English language.
+ Organizational, time management and problem-solving skills
+ Ability to establish and maintain effect...