Experienced Clinical Research Associate

Senior 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
• Requires at least 3 year of on-site monitoring experience.
• Very good computer skills including MS Office
• Excellent command of Portuguese and English language.
• Organizational, time management and prob...