Clinical Research Associate 1 - CFSP

Clinical Research Associate

Your responsibilities will include:

• Performing site selection, initiation, monitoring, and close‑out visits after completing the training period.
• 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 a scientific discipline or health care.
• At least 6 months of experience in the Pharma Industry and/or Clinical Trials environment.
• Very good computer skills including MS Office.
• Excellent command of Spanish and English language. ...