Associate Site Manager (CRA - Monitor de Pesquisa Clinica I)

Entry-level site management role supporting clinical trial operations at investigational sites. The Associate Site Manager serves as the primary liaison between Johnson & Johnson and trial sites, ensuring protocol compliance, regulatory adherence, and operational readiness throughout trial lifecycle.

Responsibilities

• Serve as primary local contact between sponsor and investigational sites for assigned trials
• Conduct site monitoring, initiation, and close-out activities in compliance with protocols and SOPs
• Ensure site staff training completion and maintain accurate training records throughout trial phases
• Verify data accuracy, completeness, and timely query resolution; manage adverse event reporting
• Document all trial activities, prepare monitoring visit reports, and communicate status to stakeholders

Requirements

• 0–2 years of clinical trial or site management experience
• Knowledge of Good Clinical Practice (GCP) and clinical trial regulations
• Strong organizational and documentation skills
• Ability to manage multiple trial sites and stakeholders
• Proficiency with clinical trial systems and data management
• Fluency in Portuguese and English (implied by Brazil location and role)