Senior Clinical Research Associate

About the Role:

• Senior Clinical Research Associate overseeing complex clinical studies.
• Responsible for training, mentoring, and coordinating junior CRAs.
• Key liaison between investigators, site staff, and project teams.

Key Responsibilities:

• Prepare, conduct, and report site selection, initiation, monitoring, and closeout visits.
• Perform CRF reviews, source document verification, and clinical data query resolution.
• Support audit preparation and assist Regulatory Affairs teams with documentation.

Requirements:

• College or university degree in Life Sciences or equivalent experience.
• At least 3 years of independent, on-site clinical monitoring experience.
• Full professional proficiency in Spanish and English.

Benefits:

• Tailored training courses and professional mentoring for career development.
• Opportunity to develop skills in training, mentoring, and leadership.
• Exposure to complex clinical studies and potential progression to Lead Monitor.